Erbb4 co-crystal

ABSTRACT

A crystal structure of the ErbB4 kinase domain (ErbB4K), specifically the ErbB4K in liganded form as well as methods of using the same in the discovery of ErbB4 inhibitors. Disclosed further are methods of treatment of diseases mediated by inappropriate ErbB4 activity utilizing ErbB4 inhibitors identified by the methods disclosed herein.

BACKGROUND OF THE INVENTION

The present invention relates to the crystal structure of the ErbB4 kinase domain (ErbB4K), specifically the ErbB4K in liganded form as well as methods of using the same in the discovery of ErbB4 inhibitors and in the treatment of diseases mediated by inappropriate ErbB4 activity.

Abberant protein tyrosine kinase (PTK) activity has been implicated in a variety of disorders including psoriasis, rheumatoid arthritis, bronchitis, as well as cancer. Development of effective treatments for such disorders is a constant and ongoing enterprise in the medical field. The ErbB family of PTKs, which includes c-ErbB-2, EGFR, and ErbB-4, is one group of PTKs that has attracted interest as a therapeutic target. Currently, of special interest, is the role of ErbB family PTKs in hyperproliferative disorders, particularly human malignancies. Consequently, inhibition of ErbB family PTKs should provide for disorders characterized by aberrant ErbB family PTK activity. The biological role of ErbB family PTKs and their implication in various disease states is discussed, for instance in U.S. Pat. No. 5,773,476; International patent application WO99/35146; M. C Hung et al, Seminars in Oncology, 26: 4, Suppl. 12 (August) 1999, 51-59; Ulrich et al, Cell, 61:203-212, Apr. 20, 1990; Modjtahedi et al, Int'l J. of Oncology, 13: 335-342, 1998; and J. R. Woodburn, Pharmacol. Ther., 82: 2-3, 241-250, 1999.

Polypeptides, including ErbB4, have a three-dimensional structure determined by the primary amino acid sequence and the environment surrounding the polypeptide. This three-dimensional structure establishes the polypeptide's activity, stability, binding affinity, binding specificity, and other biochemical attributes. Thus, knowledge of a protein's three-dimensional structure can provide much guidance in designing agents that mimic, inhibit, or improve its biological activity in soluble or membrane bound forms.

The three-dimensional structure of a polypepetide can be determined in a number of ways. Many of the most precise methods employ X-ray crystallography (See e.g., Van Holde, (1971) Physical Biochemistry, Prentice-Hall, N.J., 221-239). This technique relies on the ability of crystalline lattices to diffract X-rays or other forms of radiation. Diffraction experiments suitable for determining the three-dimensional structure of macromolecules typically require high-quality crystals. Since such crystals have been unavailable for ErbB4, a three-dimensional structure of ErbB4 has proven difficult to elucidate.

The present inventors have developed such crystals and have now determined the crystal structure of the nonphosphorylated human ErbB4K complexed with an irreversible inhibitor to 2.5 Å resolution. Such a crystal structure is useful in discovering compounds suitable for inhibiting ErbB4 and for treating diseases characterized by aberrant ErbB4 activity.

BRIEF SUMMARY OF THE INVENTION

In one aspect of the present invention, there is provided an ErbB4 kinase domain in liganded crystalline form, comprising the amino acid sequence of SEQ ID NO: 1 and having the structural coordinates of Table 2.

In a second aspect of the present invention, there is provided a method of ErbB4 inhibitor design, comprising:

generating a three dimensional computer model which represents ErbB4 kinase domain in liganded form, said kinase domain described by the amino acid sequence of SEQ ID NO: 1 and having the structural coordinates of Table 2;

evaluating compounds as potential ErbB4 inhibitors using said model; and

selecting compounds for further testing based on said evaluation.

In a third aspect of the present invention, there is provided a method of ErbB4 inhibitor design, comprising:

generating a three dimensional computer model which represents an ErbB4 kinase domain in liganded form, said kinase domain described by the amino acid sequence of SEQ ID NO: 1 and having the structural coordinates of Table 2;

evaluating compounds as potential ErbB4 inhibitors using said model; wherein said evaluation comprises identifying compounds capable of at least one of the following ErbB4 kinase domain/compound interactions:

-   -   (i) one or more interactions with amino acid residues of the         ErbB4 kinase domain hinge region;     -   (ii) one or more interactions with amino acid residues of the         ErbB4 kinase domain adenine pocket,     -   (iii) one or more interactions with amino acid residues of the         ErbB4 kinase sugar pocket,     -   (iv) one or more interactions with amino acid residues of the         ErbB4 kinase domain back pocket, and     -   (v) one or more interactions with amino acid residues of the         ErbB4 kinase domain solvent interface; and     -   selecting compounds for further testing based on said         evaluation.

In a fourth aspect of the present invention, there is provided a method of ErbB4 inhibitor design, comprising:

generating a three dimensional computer model which represents a ErbB4 kinase domain in liganded form, said kinase domain described by the amino acid sequence of SEQ ID NO: 1 and having the structural coordinates of Table 2;

evaluating compounds as potential ErbB4 inhibitors using said model; wherein said evaluation comprises identifying compounds capable of at least one of the following ErbB4 kinase domain/compound interactions:

(i) one or more interactions with amino acid residues 796, 797, 798, 799, and 800;

(ii) one or more interactions with amino acid residues 724, 749, and 850;

(iii) one or more interactions with amino acid residues 848, 860, 803, 847, 732, and 725;

(iv) one or more interactions with amino acid residues 732, 749, 751, 796, 861, 860, 772, 781, 783, 794, 796, and 862; and

(v) one or more interactions with residues 801, 802, 803, 806, and 810; and

selecting compounds for further testing based on said evaluation.

In a fifth aspect of the present invention, there is provided a method of treating a disorder characterized by inappropriate ErbB4 activity in a mammal, comprising: administering to said mammal a therapeutically effective amount of a compound that can form a complex with an ErbB4 kinase domain thereby resulting in a ErbB4 kinase domain in liganded form, said kinase domain in liganded form being described by the amino acid sequence of SEQ ID NO: 1 and the structural coordinates of Table 2, wherein said complex is characterized by at least one of the following ErbB4 kinase domain/compound interactions:

(i) one or more interactions with amino acid residues of the ErbB4 kinase domain hinge region;

(ii) one or more interactions with amino acid residues of the ErbB4 kinase domain adenine pocket,

(iii) one or more interactions with amino acid residues of the ErbB4 kinase sugar pocket and phosphate region,

(iv) one or more interactions with amino acid residues of the ErbB4 kinase domain back pocket, and

(v) one or more interactions with amino acid residues of the ErbB4 kinase domain solvent interface.

In a sixth aspect of the present invention, there is provided a method of inhibiting ErbB4 in a mammal, comprising: administering to said mammal a therapeutically effective amount of a compound that can form a complex with a ErbB4 kinase domain thereby resulting in an ErbB4 kinase domain in liganded form, said kinase domain in liganded form being described by the amino acid sequence of SEQ ID NO: 1 and the structural coordinates of Table 2, wherein said complex is characterized by at least one of the following ErbB4 kinase domain/compound interactions:

(i) one or more interactions with amino acid residues of the ErbB4 kinase domain hinge region;

(ii) one or more interactions with amino acid residues of the ErbB4 kinase domain adenine pocket,

(iii) one or more interactions with amino acid residues of the ErbB4 kinase sugar pocket and phosphate region,

(iv) one or more interactions with amino acid residues of the ErbB4 kinase domain back pocket, and

(v) one or more interactions with amino acid residues of the ErbB4 kinase domain solvent interface.

In a seventh aspect of the present invention, there is provided an ErbB4 kinase domain/inhibitor complex, comprising: an ErbB4 kinase domain form being described by the amino acid sequence of SEQ ID NO: 1 and the structural coordinates of Table 2 and a compound that can form a complex with the ErbB4 kinase domain said complex is characterized by at least one of the following ErbB4 kinase domain/compound interactions:

(i) one or more interactions with amino acid residues of the ErbB4 kinase domain hinge region;

(ii) one or more interactions with amino acid residues of the ErbB4 kinase domain adenine pocket,

(iii) one or more interactions with amino acid residues of the ErbB4 kinase sugar pocket and phosphate region,

(iv) one or more interactions with amino acid residues of the ErbB4 kinase domain back pocket, and

(v) one or more interactions with amino acid residues of the ErbB4 kinase domain solvent interface.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts the structure of two thienopyrimidine inhibitors before reaction with the protein.

FIG. 2 depicts a ribbon representation of the ErbB4K complexed with an irreversible inhibitor. A loop that is disordered in the crystal structure is shown as a dashed line. The figure was prepared with RIBBONS.

FIG. 3 depicts the binding of a thienopyrimidine inhibitor in the ATP binding site of ErbB4K. The inhibitor is highlighted with thick black lines. The hydrogen bond between the inhibitor and the backbone NH of Met799 is shown as a grey dashed line. The covalent bond between the inhibitor and Cys803 is shown as a black dashed line. The figure was created with QUANTA.

DETAILED DESCRIPTION OF THE INVENTION

Table 1 is a table summarizing the crystal and data statistics obtained from ErbB4K crystal forms. Data on the unit cell is presented, including data on the crystal space group, unit cell dimensions, molecules per asymmetric cell and crystal resolution.

Table 2 is a table of the atomic structure coordinate data obtained from X-ray diffraction from the liganded ErbB4K crystal form.

As used herein, the term “effective amount” means that amount of a drug or pharmaceutical agent that will elicit the biological or medical response of a tissue, system, animal or human that is being sought, for instance, by a researcher or clinician. Furthermore, the term “therapeutically effective amount” means any amount which, as compared to a corresponding subject who has not received such amount, results in improved treatment, healing, prevention, or amelioration of a disease, disorder, or side effect, or a decrease in the rate of advancement of a disease or disorder. The term also includes within its scope amounts effective to enhance normal physiological function.

As used herein, the term “mutation” carries its traditional connotation and means a change, inherited, naturally occurring or introduced, in a nucleic acid or polypeptide sequence, and is used in its sense as generally known to those of skill in the art.

As used herein, the term “labeled” means the attachment of a moiety, capable of detection by spectroscopic, radiologic or other methods, to a probe molecule.

As used herein, the term “target cell” refers to a cell, into which it is desired to insert a nucleic acid sequence or polypeptide, or to otherwise effect a modification from conditions known to be standard in the unmodified cell. A nucleic acid sequence introduced into a target cell can be of variable length. Additionally, a nucleic acid sequence can enter a target cell as a component of a plasmid or other vector or as a naked sequence.

As used herein, the term “transcription” means a cellular process involving the interaction of an RNA polymerase with a gene that directs the expression as RNA of the structural information present in the coding sequences of the gene. The process includes, but is not limited to, the following steps: (a) the transcription initiation, (b) transcript elongation, (c) transcript splicing, (d) transcript capping, (e) transcript termination, (f) transcript polyadenylation, (g) nuclear export of the transcript, (h) transcript editing, and (i) stabilizing the transcript.

As used herein, the term “expression” generally refers to the cellular processes by which a biologically active polypeptide is produced from RNA.

As used herein, the term “transcription factor” means a cytoplasmic or nuclear protein which binds to a gene, or binds to an RNA transcript of such gene, or binds to another protein which binds to such gene or such RNA transcript or another protein which in turn binds to such gene or such RNA transcript, so as to thereby modulate expression of the gene. Such modulation can additionally be achieved by other mechanisms; the essence of “transcription factor for a gene” is that the level of transcription of the gene is altered in some way.

As used herein, the term “hybridization” means the binding of a probe molecule, a molecule to which a detectable moiety has been bound, to a target sample.

As used herein, the term “detecting” means confirming the presence of a target entity by observing the occurrence of a detectable signal, such as a radiologic or spectroscopic signal that will appear exclusively in the presence of the target entity.

As used herein, the term “sequencing” means determining the ordered linear sequence of nucleic acids or amino acids of a DNA or protein target sample, using conventional manual or automated laboratory techniques.

As used herein, the term “isolated” means for example oligonucleotides substantially free of other nucleic acids, proteins, lipids, carbohydrates or other materials with which they can be associated, such association being either in cellular material or in a synthesis medium. The term can also be applied to other molecule types including polypeptides, in which case the polypeptide will be substantially free of nucleic acids, carbohydrates, lipids and other undesired polypeptides.

As used herein, the term “substantially pure” means that the polynucleotide or polypeptide is substantially free of the sequences and molecules with which it is associated in its natural state, and those molecules used in the isolation procedure. The term “substantially free” means that the sample is at least 50%, preferably at least 70%, more preferably 80% and most preferably 90% free of the materials and compounds with which it is associated in nature.

As used herein, the term “primer” means a sequence comprising two or more deoxyribonucleotides or ribonucleotides, preferably more than three, and more preferably more than eight and most preferably at least about 20 nucleotides of an exonic or intronic region. Such oligonucleotides are preferably between ten and thirty bases in length.

As used herein, the term “DNA segment” means a DNA molecule that has been isolated free of total genomic DNA of a particular species. For example, a DNA segment encoding a erbB4 or erbB4K polypeptide refers to a DNA segment that encodes SEQ ID NO: 1 yet is isolated away from, or purified free from, total genomic DNA of a source species, such as Homo sapiens. Included within the term “DNA segment” are DNA segments and smaller fragments of such segments, and also recombinant vectors, including, for example, plasmids, cosmids, phages, viruses, and the like.

As used herein, the phrase “enhancer-promoter” means a composite unit that contains both enhancer and promoter elements. An enhancer-promoter is operatively linked to a coding sequence that encodes at least one gene product.

As used herein, the phrase “operatively linked” means that an enhancer-promoter is connected to a coding sequence in such a way that the transcription of that coding sequence is controlled and regulated by that enhancer-promoter. Techniques for operatively linking an enhancer-promoter to a coding sequence are well known in the art; the precise orientation and location relative to a coding sequence of interest is dependent, inter alia, upon the specific nature of the enhancer-promoter.

As used herein, the term “inhibitor candidate” means a substance that is believed to interact with another moiety, for example a given ligand that is believed to interact to at least partially inhibit the activity of a complete enzyme or enzyme polypeptide, or fragment thereof, and which can be subsequently evaluated for such an interaction and activity inhibition. In a like manner, the term “ErbB4 inhibitor candidate” means a substance that is believed to interact with another moiety, for example a given ligand that is believed to interact to at least partially inhibit the activity of a complete ErbB4 or ErbB4 polypeptide, or fragment thereof, and which can be subsequently evaluated for such an interaction and activity inhibition. Representative candidate compounds or substrates include xenobiotics such as drugs and other therapeutic agents, carcinogens and environmental pollutants, natural products and extracts, as well as endobiotics such as steroids, fatty acids and prostaglandins. Other examples of candidate substances that can be investigated using the methods of the present invention include, but are not restricted to, agonists and antagonists of a ErbB4 or ErbB4 polypeptide, toxins and venoms, viral epitopes, hormones (e.g., opioid peptides, steroids, etc.), hormone receptors, peptides, enzymes, enzyme substrates, co-factors, lectins, sugars, oligonucleotides or nucleic acids, oligosaccharides, proteins, small molecules and monoclonal antibodies.

As used herein, the term “modified” means an alteration from an entity's normally occurring state. An entity can be modified by removing discrete chemical units or by adding discrete chemical units. The term “modified” encompasses detectable labels as well as those entities added as aids in purification.

As used herein, the term “interaction” means any relationship between atoms or molecules whereby atomic and/or molecular conditions or forces exist which promote binding equilibrium between such atoms or molecules. Suitable examples include, but are not limited to covalent, electrostatic, hydrophobic, hydrophilic, hydrogen, and van der Waals bonding. The nature of such bonding relationships is known in the art and is described for instance in Mathews et al (1990) Biochemistry, Chapter 2, pgs 30-54.

As used herein, the terms “structure coordinates” and “structural coordinates” are interchangeable and mean mathematical coordinates derived from mathematical equations related to the patterns obtained on diffraction of a monochromatic beam of X-rays by the atoms (scattering centers) of a molecule, for instance ErbB4K, in crystal form. The diffraction data are used to calculate an electron density map of the repeating unit of the crystal. The electron density maps are used to establish the positions of the individual atoms within the unit cell of the crystal. Those of skill in the art understand that a set of structure coordinates determined by X-ray crystallography is not without standard error. For the purpose of this invention, any set of structure coordinates for ErbB4 or a ErbB4K mutant that have a root mean square (RMS) deviation from ideal of no more than 1.5 Å, when superimposed using the polypeptide backbone atoms on the structure coordinates listed in Table 2, shall be considered identical, except that for the activation loop and nucleotide binding loop such deviation from ideal have a RMS of no more than 10 Å.

As used herein, the term “asymmetric unit” means part of a symmetric object from which the whole is built up by repeats. Thus, it is the smallest unit from which the object can be generated by the symmetry operations of its point group.

As used herein, the term “molecular replacement” means a method that involves generating a preliminary model of ErbB4 or ErbB4K mutant crystal whose structure coordinates are unknown, by orienting and positioning a molecule whose structure coordinates are known within the unit cell of the unknown crystal so as best to account for the observed diffraction pattern of the unknown crystal. Phases can then be calculated from this model and combined with the observed amplitudes to give an approximate Fourier synthesis of the structure whose coordinates are unknown. This, in turn, can be subject to any of the several forms of refinement to provide a final, accurate structure of the unknown crystal (Lattman, (1985) in Methods in Enzymology, t15: 55-77). Using the structure coordinates of erbB4K and erbB4K in liganded form provided by this invention, molecular replacement can be used to determine the structure coordinates of a crystalline mutant or homologue of ErbB4K or of a different crystal form of ErbBK.

As used herein, the terms “α-sheet” and “beta sheet” are interchangeable and mean the conformation of a polypeptide chain stretched into an extended zig-zig conformation. Portions of polypeptide chains that run “parallel” all run in the same direction. Polypeptide chains that are “antiparallel” run in the opposite direction from the parallel chains.

As used herein, the terms “α-helix” and “alpha helix” are interchangeable and mean the conformation of a polypeptide chain wherein the polypeptide backbone is wound around the long axis of the molecule in a left-handed or right-handed direction. The substituent groups of the amino acids protrude outward from the helical backbone, wherein the repeating unit of the structure is a single turn of the helix, which extends about 0.56 nm along the long axis.

As used herein, the term “mutant” means a polypeptide which is obtained by replacing at least one amino acid residue in a native erbB4 or erbB4K polypeptide with a different amino acid residue and/or by adding and/or deleting amino acid residues within the native polypeptide or at the N- and/or C-terminus of a polypeptide corresponding to a native erbB4 or erbB4K and which has substantially the same three-dimensional structure as the native erbB4 or erbB4K from which it is derived. By having substantially the same three-dimensional structure is meant having a set of atomic structure coordinates that have a root mean square deviation (RMS deviation) of less than or equal to about 1.5 Å, (10 Å for the activation loop and nucleotide binding loop) when superimposed with the atomic structure coordinates of the native erbB4 or erbB4K from which the mutant is derived when at least about 50% to 100% of the Cα atoms of the native erbB4 or erbB4K are included in the superposition. A mutant can have, but need not have, autophosphorylation activity.

As used herein, the term “space group” means a group or array of operations consistent with an infinitely extended regularly repeating pattern. It is the symmetry of a three-dimensional structure, or the arrangement of symmetry elements of a crystal. There are 230 space group symmetries possible; however, there are only 65 space group symmetries available for biological structures.

As used herein, the term “symmetry” means some spatial manipulation of an object resulting in an indistinguishable object. A symmetric object can, therefore, be superimposed on itself by some operation.

As used herein, the term “unit cell” means the fundamental portion of a crystal structure that is repeated infinitely by translation in three dimensions. A unit cell is characterized by three vectors a, b, and c, not located in one plane, which form the edges of a parallelepiped. Angles α, β and γ define the angles between the vectors: angle α is the angle between vectors b and c; angle β is the angle between vectors a and c; and angle γ is the angle between vectors a and b. The entire volume of a crystal can be constructed by regular assembly of unit cells; each unit cell comprises a complete representation of the unit of pattern, the repetition of which builds up the crystal.

As used herein, “monoclinic unit cell” means a unit cell wherein a≠b≠c and α=γ=90° and β≠90°. The vectors a, b and c describe the unit cell edges and the angles α, β, and γ describe the unit cell angles.

As used herein, “orthorhombic unit cell” means a unit cell wherein a≠b≠c; and α=β=γ=90°. The vectors a, b and c describe the unit cell edges and the angles α, β, and γ describe the unit cell angles.

As used herein, the term “crystal lattice” means the array of points defined by the vertices of packed unit cells.

As used herein, the term “active site” means that site in the erbB4K domain where substrate peptide binding, ATP binding and catalysis occur. For erbB4, the active site comprises at least the activation loop and the nucleotide binding loop.

As used herein, the term “activation loop” refers to a loop in tyrosine kinase domains between the conserved AspPheGly sequence and the conserved AlaProGlu sequence that is believed to act as a regulatory loop.

As used herein the terms “nucleotide-binding loop” and “glycine-rich loop” are synonomous and mean a loop in an RTK which contains the protein kinase-conserved glycine-rich consensus sequence.

As used herein, the term “autophosphorylation site” means a residue or residues in erbB4K that is phosphorylated by a domain of erbB4 itself.

As used herein the term “juxtamembrane region” means that portion of erbB4K located between the transmembrane helix and the tyrosine kinase domain.

As used herein, the terms “kinase insert” and “kinase insert domain” are synonymous and mean an additional domain not found in non-receptor tyrosine kinases or serine/threonine kinases. It is found between helices αD and αE in the C-terminal domain of receptor tyrosine kinases and can vary greatly in sequence and length.

As used herein, the term “C-terminal tail” means that region of an RTK that extends beyond the final helix of the C-terminal domain of the RTK.

As used herein, the term “N-terminal domain” means that region of an RTK that has a defined structure and precedes in sequence the hinge region.

As used herein, the term “modulate” means an increase, decrease, or other alteration of any or all chemical and biological activities or properties of a wild-type or mutant erbB4 or erbB4K polypeptide.

Description of ErbB4K Structure

The overall architecture of ErbB4K was analogous to structures reported previously for both serine/threonine and tyrosine protein kinases (Johnson et al, Cell, 85: 149-158; Cox et al, Curr. Opin. Struct. Biol., 4: 893-901). A C_(α) trace of ErbB4 is shown in FIG. 2, where kinase secondary structural elements are labeled according to the convention originally given for cAPK (Knighton et al, Science, 253:407-413). ErbB4K folds into two domains, with catalysis occurring in a cleft between the two domains. Residues in the N-terminal domain are primarily responsible for ligating ATP, while residues in the C-terminal domain are involved in catalysis and substrate binding.

The N-terminal domain (residues 690-801) folds into a twisted β-sheet and one α-helix. The larger C-terminal domain (residues 802-999) contains eight α-helices (αD-αI) and a set of anti-parallel β-strands (β6/β7). Strands 6 and 7 are positioned at the interdomain interface adjacent to the N-terminal β-sheet. Like other kinases, ErbB4K also contains functionally important loop regions: the glycine-rich nucleotide binding loop (residues 725-730), the catalytic loop (residues 841-848) and the activation loop (residues 861-890), which will be described in further detail below.

Activation Loop

Protein kinases contain a large flexible loop, called the activation loop or A-loop, whose conformation is believed to regulate kinase activity. In many kinases, the conformation of the A-loop is controlled by the phosphorylation of specific residues within this region (Johnson et al). The activation loop generally begins with a conserved AspPheGly sequence (ErbB4K 861) and ends at a conserved AlaProGlu (ErbB4K 890, AlaLeuGlu in ErbB4K) (Johnson et al). In structures of inactive kinases, portions of this loop are often disordered. In those structures where the A loop is ordered, it often blocks either the substrate or ATP binding sites (Mohammadi et al; Wybenga-Groot et al; Hubbard et al—1997; Hubbard et al—1994; McTigue et al; and Xu et al). Upon phosphorylation, the A-loop is repositioned to contact residues in the C-terminal domain (Hubbard et al—1997). The activating phosphate can then interact with a cluster of basic residues, which includes a conserved arginine (ErbB4K R⁸⁴²), that precedes the catalytic aspartate (ErbB4K D843). The aspartyl residue of the AspPheGly motif ligates a Mg²⁺ ion, which, in turn contacts the β and γ phosphates of ATP.

In ErbB4K, the activation loop corresponds to residues 861-890 and contains a single tyrosine at position 875. In the ErbB4K structure presented, the A-loop is completely ordered and does not significantly block either the ATP or substrate binding sites. Unlike other A loops observed to date, the A loop in ErbB4 contains a short helix (helix A) immediately following the AspPheGly motif.

In ErbB4, TyR⁸⁷⁵ is found in a similar position within the A-loop as tyrosines required for activation of other tyrosine kinases. The side chain of this residue in the ErbB4K crystal structure is pointing towards the interior of the protein rather than solvent and its OH forms a hydrogen bond to the backbone carbonyl of Cys891. It is not clear whether phosphorylation of this tyrosine in ErbB4 is required for full activity of the kinase.

Nucleotide Binding Loop

The nucleotide binding loop (NB loop) contains residues responsible for binding the triphosphate moiety of ATP in the correct position for catalysis (Johnson etal and Cox et al). This glycine-rich loop is believed to be quite flexible and is often either disordered or has high b-factors in many unliganded kinase structures sites (Mohammadi et al; Wybenga-Groot et al; Hubbard et al—1997; Hubbard et al—1994; McTigue et al; and Xu et al). In ErbB4K, this loop is ordered and occupies a similar position to that seen in other kinase structures.

Catalytic Loop

The catalytic loop of protein kinases lies between αE and β7 and contains an invariant aspartic acid (D843 in ErbB4) that serves as the catalytic base in the phosphotransfer reaction (Johnson et al). The sequence (HRDLAARN), as well as the backbone and side chain positions of this loop are similar to those in the unliganded EphB2, FGFR¹, Tie2, IRK and VEGFR² and in the ternary phosphorylated IRK complex structures sites (Mohammadi et al; Wybenga-Groot et al; Hubbard et al—1997; Hubbard et al—1994; and McTigue et al).

Inhibitor Binding Site

The ATP binding site can be broken down into several regions: hinge, adenine pocket, solvent interface, back pocket and sugar pocket. ATP is modeled into ErbB4 based on the activated IR structure. The hinge region runs from thR⁷⁹⁶ to pro800 and would be expected to form hydrogen bonds with the adenine base of ATP. The adenine pocket would be formed by the hinge residues on the side and ala749 and leu724 on top and leu850 on the bottom. The back pocket in ErbB4 is an elongated channel that can be divided by 2 regions defined by (1) val732, ala749, lys751, thR⁷⁹⁶, asp861, and thR⁸⁶⁰, and (2) met772, val781, leu783, leu794, thR⁷⁹⁶, and phe862. Typically, potential inhibitors bind in region (1) and do not reach back into region (2). A surface at the solvent interface formed by residues his801, gly802, cys803, glu806, and glu810 could form interactions with inhibitors. The ribose or sugar pocket is defined by asn848, thR⁸⁶⁰, cys803, arg847, val732, and gly725.

Inhibitor/ErbB4K Complex Structure

The structure of nonphosphorylated ErbB4 was solved in the presence of a thienopyrimidine inhibitor (formula Ia):

The inhibitor binds in the ATP binding site tunneling into the back of the pocket. The thienopyrimidine group, like the adenosine base of ATP, hydrogen bonds to the hinge region between the N and C-terminal domains (FIG. 3). The inhibitor makes a single hydrogen bond to the protein. N1 of the inhibitor hydrogen bonds to the backbone NH of Met799. The thienopyrimidine ring is sandwiched from the top and bottom by the side chains of Ala749 and Leu850, respectively. The side chain of cys803 adds into the alkynyl group forming a cis double bond. The B and C rings of the inhibitor lie deep in the back of the ATP binding site. The B ring packs against the side chains of Val732, Ala749, Lys751, ThR⁷⁹⁶, and ThR⁸⁶⁰, while the C ring sits in a hydrophobic pocket formed by Met772, Val781, Leu783, Leu794, ThR⁷⁹⁶, and Phe862.

Co-crystal structures were also solved using the thienopyrimidine compound of formula (Ib):

Further compounds which may be co-crystallized with the ErbB4 kinase domain include compounds of formula (I):

wherein: one of A¹ and A² is S and the other is CH; R¹ is H or —(CR¹¹R¹¹)_(n)—R⁵; R² is H or C₁₋₆alkyl; R³ is selected from the group consisting of aryl optionally substituted with one or more substituents selected from the group consisting of halo, alkynyl, —CF₃, —(CH₂)_(n)OR⁴, —(CH₂)_(n)SR⁴, —NO₂, C₁₋₆alkyl, —CN, —SO₂R⁹, —(CH₂)_(n)aryl and —(CH₂)_(n)NR⁹R¹⁰, and heteroaryl optionally substituted with one or more substituents selected from the group consisting of halo, alkynyl, —CF₃, —(CH₂)_(n)OR⁴, —(CH₂)_(n)SR⁴, —NO₂, C₁₋₆alkyl, —CN, —SO₂R⁹, —(CH₂)_(n)aryl and —(CH₂)_(n)NR⁹R¹⁰; R⁴ is selected from the group consisting of H, C₁₋₆alkyl, —(CH₂)_(n)NR⁹R¹⁰, —(CH₂)_(n)heterocyclyl, —(CH₂)_(n)aryl in which aryl is optionally substituted with one or more substituents selected from the group consisting of halo, —CF₃, C₁₋₆alkoxy, —NO₂, C₁₋₆alkyl, —CN, —SO₂R⁹, and —(CH₂)_(n)NR⁹R¹⁰, arylC₁₋₆alkenylene in which aryl is optionally substituted with one or more substituents selected from the group consisting of halo, —CF₃, C₁₋₆alkoxy, —NO₂, C₁₋₆alkyl, —CN, —SO₂R⁹, and —(CH₂)_(n)NR⁹R¹⁰, heteroarylC₁₋₆alkenylene in which heteroaryl is optionally substituted with one or more substituents selected from the group consisting of halo, —CF₃, C₁₋₆alkoxy, —NO₂, C₁₋₆alkyl, —CN, —SO₂R⁹, and —(CH₂)_(n)NR⁹R¹⁰, and —(CH₂)_(n)heteroaryl in which heteroaryl is optionally substituted with one or more substituents selected from the group consisting of halo, —CF₃, C₁₋₆alkoxy, —NO₂, C₁₋₆alkyl, —CN, —SO₂R⁹, and —(CH₂)_(n)NR⁹R¹⁰; R⁵ is selected from the group consisting of heterocyclyl, —N(R⁶)—C(O)—N(R⁶)(R⁷)—N(R⁶)—C(S)—N(R⁶)(R⁷), —N(R⁶)—C(O)—OR⁷, —N(R⁶)—C(O)—(CH₂)_(n)—R⁷—N(R⁶)—SO₂R⁶, —(CH₂)_(n)NR⁶R⁷ ₁—(CH₂)_(n)OR⁷—(CH₂)_(n)SR⁸—(CH₂)_(n)S(O)R⁸, —(CH₂)_(n)S(O)₂R⁸, —OC(O)R⁸, —OC(O)OR⁸, —C(O)NR⁶R⁷, heteroaryl optionally substituted with one or more substituents selected from the group consisting of halo, —CF₃, C₁₋₆alkoxy, —NO₂, C₁₋₆alkyl, —CN, —SO₂R⁹, and —(CH₂)_(n)NR⁹R¹⁰, and aryl optionally substituted with one or more substituents selected from the group consisting of halo, —CF₃, C₁₋₆alkoxy, —NO₂, C₁₋₆alkyl, —CN, —SO₂R⁹, and —(CH₂)_(n)NR⁹R¹⁰; R⁶ and R⁷ are independently selected from the group consisting of H, C₁₋₆alkyl, C₃₋₈cycloalkyl, heterocyclyl, —(CH₂)_(n)NR⁹R¹⁰, —(CH₂)_(n)OR⁹, —(CH₂)_(n)C(O)R⁸, —C(O)₂R⁸, —(CH₂)_(n)SR⁸, —(CH₂)_(n)S(O)R⁸, —(CH₂)_(n)S(O)₂R⁸, —(CH₂)_(n)R⁸, —(CH₂)_(n)CN, aryl optionally substituted with one or more substituents selected from the group consisting of halo, —CF₃, C₁₋₆alkoxy, —NO₂, C₁₋₆alkyl, —CN, —(CH₂)_(n)OR⁸, —(CH₂)_(n)heterocyclyl, —(CH₂)_(n)heteroaryl, —SO₂R⁹, and —(CH₂)_(n)NR⁹R¹⁰, and heteroaryl optionally substituted with one or more substituents selected from the group consisting of halo, —CF₃, C₁₋₆alkoxy, —NO₂, C₁₋₆alkyl, —CN, —(CH₂)_(n)OR⁸, —(CH₂)_(n)heterocyclyl, —(CH₂)_(n)heteroaryl, —SO₂R⁹, and —(CH₂)_(n)NR⁹R¹⁰, or R⁶ and R⁷, together with the atom to which they are attached, form a 3-8 membered ring; R⁸ is selected from the group consisting of C₁₋₆alkyl, C₃₋₈cycloalkyl, heterocyclylC₁₋₆alkylene, arylC₁₋₆alkylene wherein said aryl is optionally substituted with one or more substituents selected from the group consisting of halo, —CF₃, C₁₋₆alkoxy, —NO₂, C₁₋₆alkyl, —CN, —SO₂R⁹, and —(CH₂)_(n)NR⁹R¹⁰, and heteroarylC₁₋₆alkylene wherein said heteroaryl is optionally substituted with one or more substituents selected from the group consisting of halo, —CF₃, C₁₋₆alkoxy, —NO₂, C₁₋₆alkyl, —CN, —SO₂R⁹, and —(CH₂)_(n)NR⁹R¹⁰, aryl optionally substituted with one or more substituents selected from the group consisting of halo, —CF₃, C₁₋₆alkoxy, —NO₂, C₁₋₆alkyl, —CN, —SO₂R⁹, and —(CH₂)_(n)NR⁹R¹⁰, and heteroaryl optionally substituted with one or more substituents selected from the group consisting of halo, —CF₃, C₁₋₆alkoxy, —NO₂, C₁₋₆alkyl, —CN, —SO₂R⁹, and —(CH₂)_(n)NR⁹R¹⁰; R⁹ and R¹⁰ are independently selected from the group consisting of H, C₁₋₆alkyl, C₃₋₈cycloalkyl, and —C(O)R¹¹ or R⁹ and R¹⁰, together with the atom to which they are attached, form a 3-8 membered ring; R¹¹ is independently selected from the group consisting of H, C₁₋₆alkyl, and C₃₋₈cycloalkyl; and n is 0-6.

Such thienopyrimidines are described in U.S. Provisional Patent Application Ser. No. 60/342,207 filed Dec. 19, 2001 which was filed Dec. 13, 2002 as PCT Patent Application No. PCT/US02/39872 and published as WO 03/053446 on Jul. 3, 2003. Such applications are incorporated herein by reference to the extent they disclose and describe such thienopyrimidines as well as the making and use thereof.

As recited above, the present invention provides an ErbB4 kinase domain in liganded crystalline form. Such ErbB4 liganded kinase domain is described by the amino acid sequence of SEQ ID NO: 1 and the structural coordinates of Table 2. SEQ ID NO: 1 is encoded by the DNA sequence of SEQ ID NO: 2. In another embodiment, is an ErbB4 liganded kinase domain described by the amino acid sequence encoded by the DNA sequence of SEQ ID NO: 2 and the structural coordinates of Table 2. In a further embodiment, is a substantially pure and isolated ErbB4 liganded kinase domain described by the amino acid sequence of SEQ ID NO: 1 and the structural coordinates of Table 2. In another embodiment, is a substantially pure and isolated ErbB4 liganded kinase domain described by the amino acid sequence encoded by the DNA sequence of SEQ ID NO: 2 and the structural coordinates of Table 2.

In one embodiment the liganded ErbB4 kinase domain in crystalline form has lattice constants of a=63.95 Å, b=63.95 Å, c=163.95 Å, a=90°, β=90°, and γ=90°. In one embodiment, the liganded ErbB4 kinase domain in crystalline form has a space group of P4₃. In another embodiment, the liganded ErbB4 kinase in crystalline form has an entire NT region which is ordered. In still another embodiment, the liganded ErbB4 kinase in crystalline form has structural coordinates having a deviation from ideal with a RMS of no more than 1.5 Å except that the activation loop and/or a nucleotide binding loop have structural coordinates having a deviation from ideal with a RMS of no more than 10 Å. In a further embodiment, the liganded ErbB4 kinase in crystalline form has an activation loop and/or a nucleotide binding loop have structural coordinates having a deviation from ideal with a RMS of no more than 10 Å.

In another embodiment, there is provided an ErbB4 kinase domain/inhibitor complex which includes an ErbB4 liganded kinase domain described by the amino acid sequence of SEQ ID NO: 1 or 2 and the structural coordinates of Table 2 and a compound capable of at least one of the following interactions with the cFMS kinase domain:

(i) one or more interactions with amino acid residues of the ErbB4 kinase domain hinge region;

(ii) one or more interactions with amino acid residues of the ErbB4 kinase domain adenine pocket;

(iii) one or more interactions with amino acid residues of the ErbB4 kinase sugar pocket;

(iv) one or more interactions with amino acid residues of the ErbB4 kinase domain back pocket; and

(v) one or more interactions with amino acid residues of the ErbB4 kinase domain solvent interface;

preferably

(i) one or more interactions with amino acid residues 796, 797, 798, 799, and 800;

(ii) one or more interactions with amino acid residues 724, 749, and 850;

(iii) one or more interactions with amino acid residues 848, 860, 803, 847, 732, and 725;

(iv) one or more interactions with amino acid residues 732, 749, 751, 796, 861, 860, 772, 781, 783, 794, 796, and 862; and

(v) one or more interactions with residues 801, 802, 803, 806, and 810.

More preferred embodiments of interactions (i), (ii), (iii), (iv), and (v) are described following.

The amino acid region referred to in the interaction described in (i), which include amino acid residues 796-800, is typically referred to as the hinge region. In one embodiment, there are one or more kinase domain/compound bonding interactions with at least one of amino acid residues 796 to 800, preferably at least one of the bonding interactions is a hydrogen bonding interaction. In another embodiment, there are two or more bonding interactions with at least one of amino acid residues 796 to 800, preferably at least one of the bonding interactions is a hydrogen bonding interaction. In a further embodiment, there are three or more bonding interactions with at least one of amino acid residues 796 to 800, preferably at least one of the bonding interactions is a hydrogen bonding interaction. In a still further embodiment, there are four or more bonding interactions with at least one of amino acid residues 796 to 800, preferably at least one of the bonding interactions is a hydrogen bonding interaction.

In a preferred embodiment, there are one or more kinase domain/compound hydrogen bonding interactions with at least one of amino acid residues 796 to 800, alternatively two or more hydrogen bonding interactions with at least one of amino acid residues 796 to 800, in a further alternative embodiment three or more hydrogen bonding interactions with at least one of amino acid residues 796 to 800, and in a still further embodiment four or more bonding interactions with at least one of amino acid residues 796 to 800.

In a more preferred embodiment, there is a kinase domain/compound hydrogen bonding interaction with methionine 799, preferably one hydrogen bonding interaction with the backbone NH of methionine 799. Typically, this hydrogen bond is at a distance of 2.5 to 3.5, preferably 2.6 to 3.3, more preferably 2.8 to 3.0 Å.

In another embodiment, there is a kinase domain/compound hydrogen bonding interaction with methionine 799 and there are one or more kinase domain/compound bonding interactions with at least one of amino acid residues 796 to 800. In another embodiment, there is a kinase domain/compound hydrogen bonding interaction with methionine 799 and there are two or more bonding interactions with at least one of amino acid residues 796 to 800. In a further embodiment, there is a kinase domain/compound hydrogen bonding interaction with methionine 799 and there are three or more bonding interactions with at least one of amino acid residues 796 to 800. Finally, in a still further embodiment, there is a kinase domain/compound hydrogen bonding interaction with methionine 799 and there are four or more bonding interactions with at least one of amino acid residues 796 to 800. Preferably, the one of the hydrogen bonding interactions with methionine 799 is with the backbone NH of methionine 799. Typically, this hydrogen bond is at a distance of 2.5 to 3.5, preferably 2.6 to 3.3, more preferably 2.8 to 3.0.

The amino acid region referred to in the interaction described in (ii), which includes amino acid residues 749, 724, and 850, is commonly termed the adenine pocket. In one embodiment, there are one or more kinase domain/compound interactions with at least one of amino acid residues 749, 724, and 850, preferably two or more interactions with at least two of amino acid residues 749, 724, and 850, more preferably three or more interactions with at least three of amino acid residues 749, 724, and 850, most preferably four or more bonding interactions with amino acid residues 749, 724, and 850.

In one embodiment, there is a kinase domain/compound hydrophobic interaction with alanine 749, preferably an interaction with the side chain of alanine 749. In another embodiment, there is a kinase domain/compound interaction with leucine 724. In a further embodiment, there is a kinase domain/compound interaction with leucine 850, preferably an interaction with the side chain of leucine 850. In a more preferred embodiment, there is one kinase domain/compound interaction with at least one of alanine 749, leucine 724, and leucine 850. In a most preferred embodiment, there are two kinase domain/compound bonding interactions: (i) an interaction with the side chain of alanine 749 and ii) an interaction with the side chain of leucine 850.

The amino acid region referred to in the interactions described in (iii) describe what is commonly termed the sugar (ribose) pocket and is defined by amino acid residues 848, 860, 803, 847, 732, and 725. In one embodiment, there are one or more kinase domain/compound interactions with at least one of amino acid residues 848, 860, 803, 847, 732, and 725, preferably two or more interactions with amino acid residues 848, 860, 803, 847, 732, and 725.

In one embodiment, there is a kinase domain/compound interaction with asparagine 848. In another embodiment, there is a kinase domain/compound interaction with threonine 860. In another embodiment, there is a kinase domain/compound interaction with cysteine 803, preferably a covalent interaction between cysteine 803 and the compound, more preferably a covalent interaction between cysteine 803 and the alkynyl group of the compound forming a cis double bond. In another embodiment, there is a kinase domain/compound interaction with arginine 847. In another embodiment, there is a kinase domain/compound interaction with valine 732. In another embodiment, there is a kinase domain/compound interaction with glycine 725.

The amino acid region referred to in the interactions in (iv) described what is commonly termed the back pocket, which is formed by residues 732, 749, 751, 796, 861, 860, 772, 781, 783, 794, 796, and 862. In one embodiment, there are one or more kinase domain/compound interactions with at least one of amino acid residues 732, 749, 751, 796, 861, 860, 772, 781, 783, 794, 796, and 862, preferably two or more interactions with at least two of amino acid residues 732, 749, 751, 796, 861, 860, 772, 781, 783, 794, 796, and 862, more preferably three or more interactions with at least three of amino acid residues 732, 749, 751, 796, 861, 860, 772, 781, 783, 794, 796, and 862, still more preferably four or more bonding interactions with at least four of amino acid residues 732, 749, 751, 796, 861, 860, 772, 781, 783, 794, 796, and 862.

In one embodiment, there is a kinase domain/compound interaction with valine 732, preferably a hydrophobic interaction with valine 732. In another embodiment, there is a kinase domain/compound interaction with alanine 749, preferably a hydrophobic bonding interaction with alanine 749. In another embodiment, there is a kinase domain/compound interaction with lysine 751, preferably a hydrophobic interaction with lysine 751. In a further embodiment, there is a kinase domain/compound interaction with threonine 796, preferably a hydrophobic interaction with threonine 796. In another further embodiment, there is a kinase domain/compound hydrophobic interaction with aspartic acid 861, preferably a hydrophobic interaction with aspartic acid 861. In another embodiment, there is a kinase domain/compound interaction with threonine 860, preferably a hydrophobic interaction with threonine 860. In another embodiment, there is a kinase domain/compound interaction with methionine 772, preferably a hydrophobic interaction with methionine 772. In another embodiment, there is a kinase domain/compound interaction with valine 781, preferably a hydrophobic interaction with valine 781. In another embodiment, there is a kinase domain/compound interaction with leucine 783, preferably a hydrophobic interaction with leucine 783. In another embodiment, there is a kinase domain/compound interaction with leucine 794, preferably a hydrophobic interaction with leucine 794. In another embodiment, there is a kinase domain/compound interaction with threonine 796, preferably a hydrophobic interaction with threonine 796. In another embodiment, there is a kinase domain/compound interaction with phenylalanine 862, preferably a hydrophobic interaction with phenylalanine 862.

The amino acid region referred to in the interactions in (v) describe what is commonly termed the solvent interface, which is formed by residues 801, 802, 803, 806, and 810. In one embodiment, there are one or more kinase domain/compound interactions with at least one of amino acid residues 801, 802, 803, 806, and 810, preferably two or more interactions with at least two of amino acid residues 801, 802, 803, 806, and 810, more preferably three or more interactions with at least two of amino acid residues 801, 802, 803, 806, and 810.

In one embodiment, there is a kinase domain/compound interaction with histidine 801. In another embodiment, there is a kinase domain/compound interaction with glycine 802. In one embodiment, there is a kinase domain/compound interaction with cysteine 803. In another embodiment, there is a kinase domain/compound interactions glutamic acid 806. In a further embodiment, there is a kinase domain/compound interaction with glutamic acid 810.

The method of ErbB4 inhibitor design of the present invention includes as a first step: generating a three dimensional computer model which represents a ErbB4 kinase domain in liganded form, said kinase domain being described by the amino acid sequence of SEQ ID NO: 1 and having the structural coordinates of Table 2. Typically, such a computer model of SEQ ID NO: 1 and the structural coordinates of Table 2 is constructed utilizing a commercially available software program. Software programs for generating three-dimensional graphical representations of molecules or portions thereof from a set of structural coordinates are well known and used in the art. Suitable examples of such computer programs for viewing or otherwise manipulating protein structures include, but are not limited to, the following: Midas (University of California, San Francisco), MidasPlus (University of California, San Francisco),MOIL (Univeristy of Illinois), Yummie (Yale University), Sybyl (Tripos, Inc.), Insight/Discover (Biosym Technologies), MacroModel (Columbia University), Quanta (Molecular Simulations, Inc.), CNS (Molecular Simulations, Inc.), Cerius (Molucular Simulations, Inc.), Alchemy (Tripos, Inc.), LabVision (Tripos, Inc.), Rasmol (Glaxo Research and Development), Ribbon (University of Alabama), NAOMI (Oxford University), Explorer Eyechem (Silicon Graphics, Inc.), Univision (Cray Research), Molscript (Uppsala University), Chem-3D (Cambridge Scientific), Chain (Baylor College of Medicine), O (Uppsala University), GRASP (Columbia University), X-Plor (Molecular Simulations, Inc., Yale University), Spartan (Wavefunction, Inc.), Catalyst (Molecular Simulations, Inc.), Molcadd (Tripos, Inc.), VMD (University of Illinois/Beckman Institute), Sculpt (Interactive Simulations, Inc.), Procheck (Brookhaven National Laboratory), DGEOM (QCPE), RE_VIEW (Brunel University), Modeller (Birbeck College, University of London), Xmol (Minnesota Supercomputing Center), Protein Expert (Cambridge Scientific), HyperChem (Hypercube), MD Display (University of Washington), PKB (National Center for Biotechnology Information, NIH), ChemX (Chemical Design, Ltd.), Cameleon (Oxford Molecular, Inc.), and Iditis (Oxford Molecular, Inc.).

Once the three dimensional model of the ErbB4 kinase domain is established candidate inhibitor compounds may be evaluated utilizing the model and the selected software application. Initially, it is understood that the term “evaluate” includes within its scope, without limitation, de novo inhibitor molecular design, computer-aided optimization of known candidate inhibitors, as well as computer-based selection of candidate inhibitors. Various computational analysis methods are known in the art for the evaluation of potential binding interactions between a polypeptide binding pocket and a candidate inhibitor molecule. Such methods typically utilize at least one of the software packages recited above and are known in the art. Computational and other evaluation methods are described for instance in U.S. Pat. Nos. 6,251,620 and 6,356,845, such patents being incorporated herein by reference to the extent that they disclose computational and other evaluation methods for drug design, selection and/or optimization.

Examples of protein-inhibitor interactions which are screened for include potential covalent, electrostatic, hydrophobic, hydrophilic, van der Waals, and hydrogen bonding between the ErbB4 kinase molecule and candidate inhibitors as well as favorable candidate inhibitor conformations within the ErbB4 kinase binding pocket.

In one embodiment, evaluation of compounds as potential ErbB4 inhibitors using said model comprises identifying compounds capable of at least one of the following ErbB4 kinase domain/compound interactions:

(i) one or more interactions with amino acid residues of the ErbB4 kinase domain hinge region;

(ii) one or more interactions with amino acid residues of the ErbB4 kinase domain adenine pocket,

(iii) one or more interactions with amino acid residues of the ErbB4 kinase sugar pocket and phosphate region,

(iv) one or more interactions with amino acid residues of the ErbB4 kinase domain back pocket, and

(vi) one or more interactions with amino acid residues of the ErbB4 kinase domain solvent interface;

preferably

(i) one or more interactions with amino acid residues 796, 797, 798, 799, and 800;

(iii) one or more interactions with amino acid residues 724, 749, and 850;

(iii) one or more interactions with amino acid residues 848, 860, 803, 847, 732, and 725;

(iv) one or more interactions with amino acid residues 732, 749, 751, 796, 861, 860, 772, 781, 783, 794, 796, and 862; and

(v) one or more interactions with residues 801, 802, 803, 806, and 810.

Further preferred embodments of the interactions (i), (ii), (iii), (iv), and (v) are as described above.

If evaluation indicates that a compound shows promise as a candidate inhibitor the compounds are selected for further testing based on said evaluation. An inhibitor candidate is generally sought which can exist in a conformation, which appears to be structurally compatible with at least a part of the ErbB4 kinase domain binding pocket. Such conformation will be sterically and energetically compatible with the ErbB4 kinase domain. Typically, the above listed non-covalent or secondary bonding interactions will be important in the interaction of the candidate inhibitor and the ErbB4 kinase domain. In addition, other conformational factors include the overall three dimensional structure and orientation of the candidate inhibitor within the protein structure, especially the binding pocket as well as spacial and energetic relationships of the various functional groups of the candidate inhibitor and ErbB4 kinase domain which have potential for interaction. The further testing done typically is to evaluate the inhibitory effect on the kinase activity of ErbB4 and may take the form of enzyme or cell based assays as well as other assays known in the art for measuring the inhibitory effect on the kinase activity of ErbB4.

The present invention also provides a method of inhibiting ErbB4 in a mammal, which includes administering to said mammal a therapeutically effective amount of a compound that can form a complex with a ErbB4 kinase domain thereby resulting in a ErbB4 kinase domain in liganded form. Also provided is a method of treating a disorder characterized by inappropriate ErbB4 activity in a mammal which includes administering to said mammal a therapeutically effective amount of a compound that can form a complex with a ErbB4 kinase domain thereby resulting in a ErbB4 kinase domain in liganded form.

Compounds useful in the treatment methods of the present invention include those having interactions (i), (ii), (iii), (iv), and (v) with the ErbB4 kinase domain. Such interactions are as described above.

The inappropriate ErbB4 activity referred to herein is any ErbB4 activity that deviates from the normal ErbB4 activity expected in a particular mammalian subject. Inappropriate ErbB4 activity may take the form of, for instance, an abnormal increase in activity, or an aberration in the timing and or control of ErbB4 activity. Such inappropriate activity may result then, for example, from overexpression or mutation of the protein kinase leading to inappropriate or uncontrolled activation. Furthermore, it is also understood that unwanted ErbB4 activity may reside in an abnormal source, such as a malignancy. That is, the level of ErbB4 activity does not have to be abnormal to be considered inappropriate, rather the activity derives from an abnormal source.

While it is possible that, for use in therapy, therapeutically effective amounts of the compounds described in the present invention, as well as salts, solvates and physiologically functional derivatives thereof, may be administered as the raw chemical, it is possible to present the active ingredient as a pharmaceutical composition. Accordingly, the invention further provides pharmaceutical compositions, which include therapeutically effective amounts of the compound described herein and salts, solvates and physiological functional derivatives thereof, and one or more pharmaceutically acceptable carriers, diluents, or excipients. The compounds of the formula (I) and salts, solvates and physiological functional derivatives thereof, are as described above. The carrier(s), diluent(s) or excipient(s) must be acceptable in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof. In accordance with another aspect of the invention there is also provided a process for the preparation of a pharmaceutical formulation including admixing a compound of the present invention or salts, solvates and physiological functional derivatives thereof, with one or more pharmaceutically acceptable carriers, diluents or excipients.

Pharmaceutical formulations may be presented in unit dose forms containing a predetermined amount of active ingredient per unit dose. Such a unit may contain, for example, 0.5 mg to 1 g, preferably 1 mg to 700 mg, more preferably 5 mg to 100 mg of a compound of the present invention, depending on the condition being treated, the route of administration and the age, weight and condition of the patient, or pharmaceutical formulations may be presented in unit dose forms containing a predetermined amount of active ingredient per unit dose. Preferred unit dosage formulations are those containing a daily dose or sub-dose, as herein above recited, or an appropriate fraction thereof, of an active ingredient. Furthermore, such pharmaceutical formulations may be prepared by any of the methods well known in the pharmacy art.

Pharmaceutical formulations may be adapted for administration by any appropriate route, for example by the oral (including buccal or sublingual), rectal, nasal, topical (including buccal, sublingual or transdermal), vaginal or parenteral (including subcutaneous, intramuscular, intravenous or intradermal) route. Such formulations may be prepared by any method known in the art of pharmacy, for example by bringing into association the active ingredient with the carrier(s) or excipient(s).

Pharmaceutical formulations adapted for oral administration may be presented as discrete units such as capsules or tablets; powders or granules; solutions or suspensions in aqueous or non-aqueous liquids; edible foams or whips; or oil-in-water liquid emulsions or water-in-oil liquid emulsions.

For instance, for oral administration in the form of a tablet or capsule, the active drug component can be combined with an oral, non-toxic pharmaceutically acceptable inert carrier such as ethanol, glycerol, water and the like. Powders are prepared by comminuting the compound to a suitable fine size and mixing with a similarly comminuted pharmaceutical carrier such as an edible carbohydrate, as, for example, starch or mannitol. Flavoring, preservative, dispersing and coloring agent can also be present.

Capsules are made by preparing a powder mixture, as described above, and filling formed gelatin sheaths. Glidants and lubricants such as colloidal silica, talc, magnesium stearate, calcium stearate or solid polyethylene glycol can be added to the powder mixture before the filling operation. A disintegrating or solubilizing agent such as agar-agar, calcium carbonate or sodium carbonate can also be added to improve the availability of the medicament when the capsule is ingested.

Moreover, when desired or necessary, suitable binders, lubricants, disintegrating agents and coloring agents can also be incorporated into the mixture. Suitable binders include starch, gelatin, natural sugars such as glucose or beta-lactose, corn sweeteners, natural and synthetic gums such as acacia, tragacanth or sodium alginate, carboxymethylcellulose, polyethylene glycol, waxes and the like. Lubricants used in these dosage forms include sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride and the like. Disintegrators include, without limitation, starch, methyl cellulose, agar, bentonite, xanthan gum and the like. Tablets are formulated, for example, by preparing a powder mixture, granulating or slugging, adding a lubricant and disintegrant and pressing into tablets. A powder mixture is prepared by mixing the compound, suitably comminuted, with a diluent or base as described above, and optionally, with a binder such as carboxymethylcellulose, an aliginate, gelatin, or polyvinyl pyrrolidone, a solution retardant such as paraffin, a resorption accelerator such as a quaternary salt and/or an absorption agent such as bentonite, kaolin or dicalcium phosphate. The powder mixture can be granulated by wetting with a binder such as syrup, starch paste, acadia mucilage or solutions of cellulosic or polymeric materials and forcing through a screen. As an alternative to granulating, the powder mixture can be run through the tablet machine and the result is imperfectly formed slugs broken into granules. The granules can be lubricated to prevent sticking to the tablet forming dies by means of the addition of stearic acid, a stearate salt, talc or mineral oil. The lubricated mixture is then compressed into tablets. The compounds of the present invention can also be combined with a free flowing inert carrier and compressed into tablets directly without going through the granulating or slugging steps. A clear or opaque protective coating consisting of a sealing coat of shellac, a coating of sugar or polymeric material and a polish coating of wax can be provided. Dyestuffs can be added to these coatings to distinguish different unit dosages.

Oral fluids such as solution, syrups and elixirs can be prepared in dosage unit form so that a given quantity contains a predetermined amount of the compound. Syrups can be prepared by dissolving the compound in a suitably flavored aqueous solution, while elixirs are prepared through the use of a non-toxic alcoholic vehicle. Suspensions can be formulated by dispersing the compound in a non-toxic vehicle. Solubilizers and emulsifiers such as ethoxylated isostearyl alcohols and polyoxy ethylene sorbitol ethers, preservatives, flavor additive such as peppermint oil or natural sweeteners or saccharin or other artificial sweeteners, and the like can also be added.

Where appropriate, dosage unit formulations for oral administration can be microencapsulated. The formulation can also be prepared to prolong or sustain the release as for example by coating or embedding particulate material in polymers, wax or the like.

The compounds of the present invention, and salts, solvates and physiological functional derivatives thereof, can also be administered in the form of liposome delivery systems, such as small unilamellar vesicles, large unilamellar vesicles and multilamellar vesicles. Liposomes can be formed from a variety of phospholipids, such as cholesterol, stearylamine or phosphatidylcholines.

The compounds of the present invention and salts, solvates and physiological functional derivatives thereof may also be delivered by the use of monoclonal antibodies as individual carriers to which the compound molecules are coupled. The compounds may also be coupled with soluble polymers as targetable drug carriers. Such polymers can include polyvinylpyrrolidone, pyran copolymer, polyhydroxypropylmethacrylamidephenol, polyhydroxyethylaspartamidephenol, or polyethyleneoxidepolylysine substituted with palmitoyl residues. Furthermore, the compounds may be coupled to a class of biodegradable polymers useful in achieving controlled release of a drug, for example, polylactic acid, polepsilon caprolactone, polyhydroxy butyric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacrylates and cross-linked or amphipathic block copolymers of hydrogels.

Pharmaceutical formulations adapted for transdermal administration may be presented as discrete patches intended to remain in intimate contact with the epidermis of the recipient for a prolonged period of time. For example, the active ingredient may be delivered from the patch by iontophoresis as generally described in Pharmaceutical Research, 3(6), 318 (1986).

Pharmaceutical formulations adapted for topical administration may be formulated as ointments, creams, suspensions, lotions, powders, solutions, pastes, gels, sprays, aerosols or oils.

For treatments of the eye or other external tissues, for example mouth and skin, the formulations are preferably applied as a topical ointment or cream. When formulated in an ointment, the active ingredient may be employed with either a paraffinic or a water-miscible ointment base. Alternatively, the active ingredient may be formulated in a cream with an oil-in-water cream base or a water-in-oil base.

Pharmaceutical formulations adapted for topical administrations to the eye include eye drops wherein the active ingredient is dissolved or suspended in a suitable carrier, especially an aqueous solvent.

Pharmaceutical formulations adapted for topical administration in the mouth include lozenges, pastilles and mouth washes.

Pharmaceutical formulations adapted for rectal administration may be presented as suppositories or as enemas.

Pharmaceutical formulations adapted for nasal administration wherein the carrier is a solid include a coarse powder having a particle size for example in the range 20 to 500 microns which is administered in the manner in which snuff is taken, i.e. by rapid inhalation through the nasal passage from a container of the powder held close up to the nose. Suitable formulations wherein the carrier is a liquid, for administration as a nasal spray or as nasal drops, include aqueous or oil solutions of the active ingredient.

Pharmaceutical formulations adapted for administration by inhalation include fine particle dusts or mists, which may be generated by means of various types of metered, dose pressurised aerosols, nebulizers or insufflators.

Pharmaceutical formulations adapted for vaginal administration may be presented as pessaries, tampons, creams, gels, pastes, foams or spray formulations.

Pharmaceutical formulations adapted for parenteral administration include aqueous and non-aqueous sterile injection solutions which may contain anti-oxidants, buffers, bacteriostats and solutes which render the formulation isotonic with the blood of the intended recipient; and aqueous and non-aqueous sterile suspensions which may include suspending agents and thickening agents. The formulations may be presented in unit-dose or multi-dose containers, for example sealed ampoules and vials, and may be stored in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example water for injections, immediately prior to use. Extemporaneous injection solutions and suspensions may be prepared from sterile powders, granules and tablets.

It should be understood that in addition to the ingredients particularly mentioned above, the formulations may include other agents conventional in the art having regard to the type of formulation in question, for example those suitable for oral administration may include flavouring agents.

A therapeutically effective amount of a compound of the present invention will depend upon a number of factors including, for example, the age and weight of the animal, the precise condition requiring treatment and its severity, the nature of the formulation, and the route of administration, and will ultimately be at the discretion of the attendant physician or veterinarian. However, an effective amount of a compound of the present invention for the treatment of neoplastic growth, for example colon or breast carcinoma, will generally be in the range of 0.1 to 100 mg/kg body weight of recipient (mammal) per day and more usually in the range of 1 to 10 mg/kg body weight per day. Thus, for a 70 kg adult mammal, the actual amount per day would usually be from 70 to 700 mg and this amount may be given in a single dose per day or more usually in a number (such as two, three, four, five or six) of sub-doses per day such that the total daily dose is the same. An effective amount of a salt or solvate, or physiologically functional derivative thereof, may be determined as a proportion of the effective amount of the compound of the present invention per se. It is envisaged that similar dosages would be appropriate for treatment of the other conditions referred to above.

EXAMPLES

As used herein the symbols and conventions used in these processes, schemes and examples are consistent with those used in the contemporary scientific literature, for example, the Journal of the American Chemical Society or the Journal of Biological Chemistry. Standard single-letter or three-letter abbreviations are generally used to designate amino acid residues, which are assumed to be in the L-configuration unless otherwise noted. Unless otherwise noted, all starting materials were obtained from commercial suppliers and used without further purification.

Structure Determination

Modeling and limited proteolysis of the entire intracellular domain of ErbB4 were used to define a construct suitable for structural studies (residues 690-999). A 6×-His tag was added at the N-terminus to aid in the purification. The construct was expressed in baculovirus-infected insect cells and purified by standard chromatographic procedures. Crystallization screens were performed using nonphosphorylated protein complexed with an irreversible inhibitor (FIG. 1). Crystals were obtained in the tetragonal space group P4₃ with two molecules in the asymmetric unit.

The structure was solved by molecular replacement using the structure of the FGFR¹ as a search model [molecule 1 of PDB entry 1FGK]. The structure was refined to an R-factor of 21% at 2.5 Å resolution (Table 1). 8 residues at the N-terminus, 7 residues at the C-terminus and 6 residues within a surface exposed loop (residues 754-761) were disordered and could not be modeled. The structure of the two molecules in the asymmetric unit was essentially identical with a C_(α) rmsd of 0.20 Å.

Certain embodiments of the present invention will now be illustrated by way of example only.

Materials and Methods

Construct Generation

A combination of limited proteolysis and modeling was used to define the construct for structural studies. First, the cytoplasmic domain of ErbB4 (residues 690-1309) was ligated in frame behind a 6×His tag (MKKGHHHHHHG) in a pFastBac1 vector (Invitrogen). The cloned sequence was identical to that reported in GENBANK (L07868).

Limited proteolysis was performed on purified protein from the 6×His-EphB4_(—)690-1309 construct to define a smaller catalytic domain (see below for more details). Proteolysis suggested that both the C-terminus could be truncated. Therefore, a second construct was generated corresponding to residues 690-999 fused to a 6×his tag (MKKGHHHHHHG). The His-tagged kinase domain was cloned by PCR from the pFastBac1-His-EphB4_(—)690-1309 construct and ligated into a pFastBac1 vector (Invitrogen).

Both constructs were transfected into Spodoptera frugiperda (sf-9) cells, single plaques were isolated, and high titer stocks were generated. The proteins were expressed and purified as described below.

Limited Proteolysis

Purified 6×His-ErbB4_(—)690-1309 was digested with a panel of 8 proteases in a 96 well plate. 5 ug of 6×His-ErbB4 (5 uL at 1 mg/mL) was added to 5 uL of 10 mg/mL protease in 20 uL of reaction buffer (56 mM Tris-HCl, pH 8.0, 100 mM NaCl). Reactions were stopped at 0.75, 2, and 18 hours with 10 uL of 4×SDS-PAGE sample buffer. All digests where analyzed by SDS-PAGE (NuPAGE Novex 10% Bis-Tris gel, MES running buffer). Bands of interest were electroblotted on PVDF membrane and subjected to Edman sequencing. Source (Boehringer Mannheim Proteases used unless otherwise noted) 1.) Trypsin catalogue # 1418475 2.) Chymotrypsin catalogue # 1418467 3.) Lys C catalogue # 1047825 4.) Glu C catalogue # 1047817 5.) Asp N catalogue # 1054589 6.) Arg C catalogue # 1370529 7.) Thermolysin catalogue # 161586 8.) Subtilisin catalogue # 572908 (Calbiochem) Protein Fermentation/Purification

Fermentation: Large-scale (2L) virus preparations for fermentation were made by infecting Sf-9 cells growing in Grace's Supplemented medium (GIBCO/Life Technologies)+0.1% capluronic® F-68 (GIBCO/Life Technologies)+10% FBS (HyClone Laboratories) at a multiplicity of infection (MOI) of 0.1 in 6L shake flasks at 27.5° C. and 120 RPM. Viral supernatants were harvested at 72 hours post-infection via centrifugation at 2500 RPM for 20 minutes. Viral titers were determined via ELISA. A 36L stirred bioreactor (University Research Glassware) was outfitted with external overhead stirrer & water bath and internal dip tubes, heat-transfer coil, paddle-style impeller and dO₂ probe. The bioreactor was inoculated with Trichoplusia ni (T. ni) cells [kindly obtained from JRH BioSciences (Woodland, Calif.)] at ˜0.5×10⁶/mL. The culture was grown in Ex-Cell™ 405 insect cell medium (JRH BioSciences). Temperature was maintained at 27.5° C. using an external water bath and an internal temperature probe & heat-transfer coil. Agitation was maintained at 30 RPM using an external overhead drive and an internal paddle-type impeller. Dissolved oxygen was maintained at 50% via sparging under the control of an internal dO₂ probe. Cells were allowed to double overnight at the above parameters, and the culture was then infected at a density of ˜1×10⁶/mL at MOI=1. The culture was monitored daily for pH, glucose, lactate and glutamine levels as well as cell count and viability via trypan blue exclusion. Infection was allowed to proceed at the above parameters, and cells were harvested at 48 hours post-infection using a Centritech® 100 continuous flow centrifuge (DuPont). Concentrated cells were subsequently centrifuged at 2000 RPM for 20 minutes and washed with protease inhibitor buffer [1× Dulbecco's PBS (GIBCO/Life Technologies), 1 mM EDTA (Sigma), 1 mM p-aminobenzamidine (Sigma), 1 μg/mL aprotinin (Boehringer Mannheim), 1 μg/mL leupeptin (Boehringer Mannheim)]. Cells were centrifuged again at 2000 RPM for 20 minutes. The supernatant was decanted, and the cells were flash frozen in a dry ice/ethanol bath and stored at −80° C. until further purification.

Purification:

All operations were carried out at 4° C. Insect cells were resuspended and thawed in buffer A (25 mM HEPES pH 7.5, 750 mM NaCl, 10% glycerol, 25 mM imidazole) supplemented with a protease inhibitor cocktail (Sigma), 1 mM MgCl₂ and 5 μg/ml of DNAse I and RNAse. The cells were lysed with a Polytron homogenizer (Brinkmann) and then centrifuged for 1 hour at 30,000 g (14,000 rpm) in a Sorvall SLA 1500 rotor. The pelleted material was discarded, and the supernatant was filtered through a 4.5μ filter (PALL Corp.). The lysate was directly loaded onto a Ni-Chelating Sepharose FF column (Amersham Pharmacia). Before sample loading, the column was equilibrated with 5 column volumes (CV's) of buffer A. After sample loading, the column was washed for 5 CV's with buffer A. The protein was eluted with a 20 CV linear gradient from 50 to 500 mM imidazole in buffer A. Fractions containing ErbB4K protein were analyzed by polyacrylamide gel electrophoresis and pooled. The pool was diluted 8 fold in Buffer B (20 mM HEPES, 20 mM NaH₂PO₄, pH 6.8, 10% glycerol) and loaded onto Ceramic HA (Bio-Rad) column previously equilibrated in buffer B. Active ErbB4 flows through and does not bind. The flow-through fraction was brought to 0.6M (NH₄)₂SO₄ by addition of a 2.5M (NH₄)₂SO₄ stock solution and the sample applied to a Phenyl HIC column previously equilibrated in buffer E (20 mM Tris-HCl, pH 7.5, 0.6M (NH₄)₂SO₄). A reverse linear gradient to 100% buffer F (20 mM Tris-HCl, pH 7.5, 10% glycerol) was used to elute protein. Fractions containing pure ErbB4 were pooled, aliquoted and stored at −80° C.

Preparation of Inhibitor Candidate Compounds

As used herein the symbols and conventions used in these processes, schemes and examples are consistent with those used in the contemporary scientific literature, for example, the Journal of the American Chemical Society or the Journal of Biological Chemistry. Standard single-letter or three-letter abbreviations are generally used to designate amino acid residues, which are assumed to be in the L-configuration unless otherwise noted. Unless otherwise noted, all starting materials were obtained from commercial suppliers and used without further purification. Specifically, the following abbreviations may be used in the examples and throughout the specification:

g (grams); mg (milligrams);

L (liters); mL (milliliters);

μL (microliters); psi (pounds per square inch);

M (molar); mM (millimolar);

mol (moles); mmol (millimoles);

All references to ether are to diethyl ether; brine refers to a saturated aqueous solution of NaCl. Unless otherwise indicated, all temperatures are expressed in ° C. (degrees Centigrade). All reactions are conducted under an inert atmosphere at room temperature unless otherwise noted.

¹H NMR spectra were recorded on a Varian VXR-300, a Varian Unity-300, a Varian Unity-400 instrument, a Brucker AVANCE-400, or a General Electric QE-300. Chemical shifts are expressed in parts per million (ppm, 8 units). Coupling constants are in units of hertz (Hz). Splitting patterns describe apparent multiplicities and are designated as s (singlet), d (doublet), t (triplet), q (quartet), quint (quintet), m (multiplet), br (broad).

HPLC were recorded on a Gilson HPLC or Shimazu HPLC system by the following conditions. Column: 50×4.6 mm (id) stainless steel packed with 5 μm Phenomenex Luna C-18; Flow rate: 2.0 mL/min; Mobile phase: A phase=50 mM ammonium acetate (pH 7.4), B phase=acetonitrile, 0-0.5 min (A: 100%, B: 0%), 0.5-3.0 min (A:100-0%, B:0-100%), 3.0-3.5 min (A: 0%, B: 100%), 3.5-3.7 min (A: 0-100%, B: 100-0%), 3.7-4.5 min (A: 100%, B: 0%); Detection: UV 254 nm; Injection volume: 3 μL.

Low-resolution mass spectra (MS) were recorded on a JOEL JMS-ΔX505HA, JOEL SX-102, or a SCIEX-APIiii spectrometer; LC-MS were recorded on a micromass 2MD and Waters 2690; high resolution MS were obtained using a JOEL SX-102A spectrometer. All mass spectra were taken under electrospray ionization (ESI), chemical ionization (CI), electron impact (EI) or by fast atom bombardment (FAB) methods. Infrared (1R) spectra were obtained on a Nicolet 510 FT-IR spectrometer using a 1-mm NaCl cell. Most of the reactions were monitored by thin-layer chromatography on 0.25 mm E. Merck silica gel plates (60F-254), visualized with UV light, 5% ethanolic phosphomolybdic acid or p-anisaldehyde solution. Flash column chromatography was performed on silica gel (230-400 mesh, Merck).

Compounds of Formula I(a) and I(b) can be prepared according to the synthetic sequence detailed in the Examples section following.

Example 1 N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-6-ethynylthieno[3,2-d]pyrimidin-4-amine

Step A

Preparation of 6-Bromo-N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}thieno[3,2-d]pyrimidin-4-amine hydrochloride

6-Bromo-4-chlorothieno[3,2-d]pyrimidine (2) (1.05 g, 4 mmol) and 3-chloro-4-[(3-fluorobenzyl)oxy]aniline (986 mg, 3.9 mmol) were heated at 60° C. for 3 h in isopropanol (30 mL). The mixture was concentrated and the resulting material was triturated with ethyl ether and collected by suction filtration to yield the product (1.7 g) as a white solid.

Step B

Preparation of N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-6-ethynylthieno[3,2-d]pyrimidin-4-amine

6-Bromo-N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}thieno[3,2-d]pyrimidin-4-amine hydrochloride (1.0 g, 2.0 mmol) was combined with CuI (45 mg, 0.24 mmol), dichlorobis(triphenylphosphine)palladium(II) (57 mg, 0.08 mmol), THF (14 mL), triethylamine (0.74 mL, 5.3 mmol), and trimethylsilylacetylene (0.37 mL, 2.62 mmol). The mixture stirred at room temperature for 6 h, concentrated and purified by silica gel chromatography (eluting with 3:1 to 2:1 hexane/ethyl acetate). The resulting silyl acetylene intermediate (618 mg) was dissolved in THF (17 mL) and cooled to 0° C. A 1.0 M solution of TBAF in THF (1.4 mL, 1.4 mmol) was added and the mixture was stirred 1 h. The reaction was partitioned between ethyl acetate and water, the organic layer was separated and dried (Na₂SO₄) filtered and concentrated. The resulting solid was purified by silica gel chromatography (eluting with 7:3 to 6:4 hexane/ethyl acetate) to give the title compound (400 mg) as an orange solid. ESI MS (positive ion): (M-H) 410.2 ¹H NMR (300 MHz, DMSO) δ 5.03 (s, 1H), 5.25 (s, 2H), 7.14-7.21 (m, 1H), 7.23-7.22 (m, 3H), 7.43-7.50 (d, 1H), 7.61 (dd, J=8.9, 2.6 Hz, 1H), 7.71 (s, 1H), 7.92 (d, J=2.5 Hz, 1H), 8.59 (s, 1H), 9.78 (s, 1H).

Example 2 N-{3-Chloro-4-[(3-fluorobenzyl)oxy]phenyl}-6-ethynylthieno[2,3-d]pyrimidin-4-amine

Step A

Preparation of 6-bromothieno[2,3-d]pyrimidin-4(3H)-one

To a slurry of commercially available thieno[2,3-d]pyrimidin-4(3H)-one (1.5 g, 9.86 mmol) in glacial acetic acid (26 mL) was added dropwise bromine (1.0 mL, 20 mmol). The dark brown mixture was heated at 80° C. for 1.5 h. The mixture was allowed to cool to ambient temperature and was poured onto a mixture of saturated aqueous NaHCO₃ and ice. The resulting solid was collected by suction filtration, washed with water and dried in vacuo to afford 2.09 g of the title compound. ¹H NMR (400 MHz, DMSO-d₆) δ 7.54 (s, 1H), 8.13 (d, 2H, J=3.7 Hz), 12.6 (bs, 1H).

Step B

Preparation of 6-Bromo-4-chlorothieno[2,3-d]pyrimidine

6-Bromothieno[2,3-d]pyrimidin-4(3H)-one (2.09 g, 9.05 mmol) was covered with phorphorous oxychloride (4.0 mL, 42.9 mmol) and the mixture was heated at 118-120° C. for 2 h. The mixture was allowed to cool to ambient temperature and was poured onto a mixture of saturated aqueous NaHCO₃ and ice. The resulting precipitate was collected by suction filtration and washed with water. The resulting solid was dried in vacuo to afford 2.07 g of the title compound. ¹H NMR (400 MHz, DMSO-d₆) δ 7.88 (s, 1H), 8.93 (s, 1H).

Step C

Preparation of 6-Bromo-N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}thieno[2,3-d]pyrimidin-4-amine

A mixture of 6-bromo-4-chlorothieno[2,3-d]pyrimidine (2.07 g, 8.29 mmol), 3-chloro-4-[(3-fluorobenzyl)oxy]aniline (2.09 g, 8.29 mmol), triethylamine (2.31 mL, 16.57 mmol) and isopropanol (40 mL) was heated at 85° C. for 16 h. The mixture was allowed to cool to ambient temperature and concentrated to leave a brown residue. The mixture was triturated with ether to afford the title compound (3.34 g) as a tan solid. ¹H NMR (400 MHz, DMSO-d₆) δ 5.24 (s, 2H), 7.18 (m, 1H), 7.26 (d, 1H, J=9.1 Hz), 7.32 (m, 1H), 7.64 (dd, 1H, J=12.1, 2.7 Hz), 8.00 (d, 1H, J=2.5 Hz), 8.02 (s, 1H), 8.48 (s, 1H), 9.63 (s, 1H).

Step D

Preparation of N-{3-Chloro-4-[(3-fluorobenzyl)oxy]phenyl}-6-[(trimethylsilyl)ethynyl]-4,4a-dihydrothieno[2,3-d]pyrimidin-4-amine

An N₂-flushed flask was charged with 6-bromo-N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}thieno[2,3-d]pyrimidin-4-amine (1.0 g, 2.15 mmol), Cu(I)I (46 mg, 0.24 mmol), dichlorobis(triphenylphosphino)palladium(II) (57 mg, 0.081 mmol), anhydrous THF (13.5 mL), triethylamine (600 μL, 4.3 mmol) and trimethylsilyl acetylene (370 μL, 2.62 mmol) and the resulting mixture was heated at 40° C. for 5 h. The mixture was concentrated with a rotary evaporator and the residue was purified by flash silica gel chromatography (eluting with 5:1 hexanes/ethyl acetate) to afford 623.4 mg of the title compound as a yellow solid. ¹H NMR (400 MHz, DMSO-d₆) δ 0.25 (s, 9H), 5.22 (s, 2H), 7.16 (dt, 1H, J=8.9, 2.5 Hz), 7.24 (d, 1H, J=9.0), 7.29 (m, 1H). 7.43 (m, 1H), 7.62 (dd, 1H, J=8.9, 2.5 Hz), 8.01 (d, 1H, J=2.8 Hz), 8.09 (s, 1H), 8.52 (s, 1H), 9.63 (s, 1H).

Step E

Preparation of N-{3-Chloro-4-[(3-fluorobenzyl)oxy]phenyl}-6-ethynylthieno[2,3-d]pyrimidin-4-amine

To a 0° C. solution of N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-6-[(trimethylsilyl)ethynyl]-4,4a-dihydrothieno[2,3-a]pyrimidin-4-amine (623.4 mg, 1.29 mmol) in anhydrous THF (17 mL) was added 1.0 M TBAF in THF (1.41 mL, 1.41 mmol). The mixture was stirred at 0° C. for 30 min, then partitioned between ethyl acetate and water. The organic layer was separated, dried over Na₂SO₄, filtered and concentrated to give a residue that was purified by silica gel chromatography (eluting with 5:1 hexanes/ethyl acetate) to give 519.3 mg of the title compound as a pale yellow solid, mp 197° C. ¹H NMR (400 MHz, DMSO-d₆) δ 4.89 (s, 1H), 5.27 (s, 2H), 7.21 (t, 1H, J=9.2 Hz), 7.31 (d, 1H, J=9.2 Hz), 7.34-7.36 (m, 1H). 7.45-7.50 (m, 1H), 7.67 (dd, 1H, J=9.0, 2.4 Hz), 8.02 (d, 1H, J=2.4 Hz), 8.10 (s, 1H), 8.56 (s, 1H), 9.75 (s, 1H). ms (MH)+=382.3.

ErbB4 Enzyme Assays:

Compounds of the present invention may be tested for ErbB-4 protein tyrosine kinase inhibitory activity in substrate phosphorylation assays using enzymes purified from a baculovirus expression system. Reagent production and assay methodology were conducted essentially as described (Brignola, P. S., et al, (2002) J. Biol. Chem. v. 277 in press).

The method measures the ability of the isolated enzyme to catalyse the transfer of the y-phosphate from ATP onto tyrosine residues in a biotinylated synthetic peptide (biotin-Ahx-RAHEEIYHFFFAKKK-amide). Reactions were performed in 96-well polystyrene round-bottom plates in a final volume of 45 μL. Reaction mixtures contained 50 mM MOPS (pH 7.5), 2 mM MnCl₂, 10 μM ATP, 0.125 μCi [γ-³³P] ATP per reaction, 2 μM peptide substrate, and 1 mM dithiothreitol. Reactions were initiated by adding 1 pmol (20 nM) per reaction of the indicated enzyme. The reaction was allowed to proceed for 15 minutes, terminated and quantified using a scintillation proximity assay procedure as described in McDonald, O. B., Antonsson, B., Arkinstal, S., Marshall, C. J., and Wood, E. R. (1999) Analytical Biochemistry, 268, 318-329.

Compounds under analysis were dissolved in Me₂SO to 0.5 mM and serially diluted 1 to 3 with Me₂SO through eleven columns of a 96 well plate. 1 μL of each concentration was transferred to the corresponding well of the assay plate. This creates a final compound concentration range from 0.00019 to 11.1 μM.

The data for dose responses were plotted as % Control calculated with the data reduction formula 100*(U1−C2)/(C1−C₂) versus concentration of compound and fitted to the curve described by: γ=((Vmax*x)/(K+x)) where Vmax is the upper asymptote and K is the IC₅₀. Typically, promising ErbB4 inhibitors will illicit a pIC50 >7.0. Crystallization and Data Collection

Crystals were obtained by the hanging drop vapor diffusion method. Protein (˜4 mg/ml in 20 mM HEPES pH 7.5, 300 mM NaCl, 5 mM DTT, 1 mM CHAPS) was mixed with an equal volume of reservoir (50 mM cacodylate pH 6.5, 100 mM ammonium acetate, 10 mM Mg acetate, 30% PEG8000) and incubated at 22° C. Crystals belonged to the tetragonal space group P43 with two molecules in the asymmetric unit and the following cell dimensions: a=63.95 Å, b=63.95 Å, c=163.39 Å, α=90°, β=90°, γ=90°.

Prior to data collection, glycerol and PEG400 was added to a final concentration of 25% and 5%, respectively, and the crystals were flash frozen in liquid N₂. Data was collected at beamline 17-BM on a MAR-CCD detector in the facilities of the Industrial Macromolecular Crystallography Association Collaborative Access Team (IMCA-CAT) at the Advanced Photon Source, Argonne National Laboratory. These facilities are supported by the companies of the Industrial Macromolecular Crystallography Association through a contract with Illinois Institute of Technology (IIT), executed through the IIT's Center for Synchrotron Radiation Research and Instrumentation. The data were processed using HKL2000.

Structure Determination and Refinement

The structure was solved by molecular replacement using CNX and FGFR¹ as a search model (molecule 1 of PDB entry 1FGK). The search model contained FGFR¹ residues 464-485, 491-500, 506-578, 592-647 and 651-761. Residues not conserved between FGFR¹ and ErbB4 were truncated to alanine in the model. The correct solutions were the top two peaks in both the rotation and translation functions. Rigid body refinement gave an initial R-factor of 48%. Multiple rounds of model building and refinement were carried out with QUANTA and CNX. The overall structure was confirmed by a composite omit map calculated with CNX. Analysis of the structure with PROCHECK indicated that all main chain torsions fall within the allowed regions of the Ramachandran plot.

The results are depicted in Table 1 and 2 following.

(1) Amino Acid Sequence: (SEQ ID NO: 1) MKKGHHHHHHGLETELVEPLTPSGTAPNQAQLRILKETELKRVKVLGSGA FGTVYKGIWVPEGETVKIPVAIKILNETTGPKANVEFMDEALIMASMDHP HLVRLLGVCLSPTIQLVTQLMPHGCLLEYVHEHKDNIGSQLLLNWCVQIA KGMMYLEERRLVHRDLAARNVLVKSPNHVKITDFGLARLLEGDEKEYNAD GGKMPIKWMALECIHYRKFTHQSDVWSYGVTIWELMTFGGKPYDGIPTRE IPDLLEKGERLPQPPICTIDVYMVMVKCWMIDADSRPKFKELAAEFSRMA RDPQRYLVIQGDDRMKLPSPNDSKFFQNLLDEEDLEDMMDAEEYLVPQAF NIPPPIYTSRARID

DNA Sequence 1: His-ErbB4Amino Acids 690-999 Nucleotide Sequence: SEQ ID No : 2 1 ATGAAAAAAG GTCATGATCA TCATCATCAT GGTTTGGAAA CAGAGTTGGT 51 GGAACCATTA AGTCCCAGTG GCACAGCACC CAATCAAGCT CAACTTCGTA 101 TTTTGAAAGA AACTGAGCTG AAGAGGGTAA AAGTCC1TGG CTCAGGTGCT 151 TTTGGAACGG TTTATAAAGG TATTTGGGTA CCTGAAGGAG AAACTGTGAA 201 GATTCCTGTG GCTATTAAGA TTCTTAATGA GACAACTGGT CCCAAGGCAA 251 ATGTGGAGTT GATGGATGAA GCTCTGATCA TGGCAAGTAT GGATCATCCA 301 CACCTAGTCC GG1TGCTGGG TGTGTGTCTG AGCCCAACCA TCCAGCTGGT 351 TACTCAACTT ATGCCCCATG GGTGCGTGTT GGAGTATGTC GAGGAGGACA 401 AGGATAACAT TGGATCACAA CTGCTGCTTA ACTGGTGTGT CCAGATAGCT 451 AAGGGAATGA TGTACCTGGA AGAAAGACGA CTCGTTCATC GGGATTTGGC 501 AGCCCGTAAT GTCTTAGTGA AATCTCCAAA CCATGTGAAA ATCACAGATT 551 TTGGGCTAGC CAGACTCTTG GAAGGAGATG AAAAAGAGTA CAATGCTGAT 601 GGAGGAAAGA TGCCAATTAA ATGGATGGCT CTGGAGTGTA TACATTACAG 651 GAAATTCACC CATCAGAGTG ACGTTTGGAG CTATGGAGTT ACTATATGGG 701 AACTGATGAC CTTTGGAGGA AAACCCTATG ATGGAATTCC AACGCGAGAA 751 ATCCCTGATT TATTAGAGAA AGGAGAACGT TTGCCTCAGG CTCCCATCTG 801 CACTATTGAC GTTTACATGG TCATGGTCAA ATGTTGGATG ATTGATGCTG 851 ACAGTAGACC TAAATTTAAG GAACTGGCTG GTGAGTTTTC AAGGATGGCT 901 CGAGACCCTC AAAGATACCT AGTTATTCAG GGTGATGATC GTATGAAGCT 951 TCCCAGTCCA AATTGA.

TABLE 1 DATA STATISTICS Space group P4₃ Unit Cell a (Å) 63.95 Unit Cell b (Å) 63.95 Unit Cell c (Å) 163.39 Unit Cell α = β = γ (°) 90 Mol/asu 2 Resolution (Å) 2.5 R_(sym) (%) 8.8 Completeness (%) 91.9 R_(factor) (%) 21 R_(free) (%) 27 Rmsd from ideal Bond lengths (Å) 0.011 Bond angles (°) 1.48

TABLE 2 erbB4(690-999) thienopyrimidine cocrystal resolution: 500.0-2.5 A sg = P4(3) a = 63.954 b = 63.954 c = 163.391 alpha = 90 beta = 90 gamma = 90 final r = 0.2130 free_r = 0.2762 rmsd bonds = 0.011188 rmsd angles = 1.48513 data completeness 91.9% Rmerge 8.8% data collected on a marCCD at IMCA, −180 C., processed with HKL2000, solved with CNX ATOM 1 N LEU A 698 −53.411 26.468 10.538 1.00 81.54 ATOM 2 CA LEU A 698 −53.129 25.423 9.504 1.00 81.33 ATOM 3 C LEU A 698 −53.233 26.015 8.103 1.00 81.09 ATOM 4 O LEU A 698 −54.198 26.709 7.791 1.00 81.42 ATOM 5 CB LEU A 698 −54.120 24.260 9.636 1.00 81.21 ATOM 6 CG LEU A 698 −53.757 22.974 8.884 1.00 81.79 ATOM 7 CD1 LEU A 698 −52.552 22.311 9.555 1.00 81.75 ATOM 8 CD2 LEU A 698 −54.949 22.024 8.877 1.00 81.23 ATOM 9 N THR A 699 −52.236 25.740 7.265 1.00 81.31 ATOM 10 CA THR A 699 −52.210 26.243 5.890 1.00 82.23 ATOM 11 C THR A 699 −51.171 25.519 5.018 1.00 82.37 ATOM 12 O THR A 699 −50.003 25.905 4.971 1.00 82.32 ATOM 13 CB THR A 699 −51.933 27.781 5.852 1.00 82.76 ATOM 14 OG1 THR A 699 −50.977 28.138 6.863 1.00 81.44 ATOM 15 CG2 THR A 699 −53.226 28.567 6.062 1.00 82.15 ATOM 16 N PRO A 700 −51.593 24.452 4.315 1.00 82.54 ATOM 17 CA PRO A 700 −50.743 23.642 3.435 1.00 82.57 ATOM 18 C PRO A 700 −49.901 24.432 2.446 1.00 82.12 ATOM 19 O PRO A 700 −50.175 25.596 2.159 1.00 82.75 ATOM 20 CB PRO A 700 −51.747 22.741 2.724 1.00 82.43 ATOM 21 CG PRO A 700 −52.758 22.504 3.777 1.00 82.66 ATOM 22 CD PRO A 700 −52.958 23.898 4.353 1.00 83.18 ATOM 23 N ALA A 701 −48.873 23.772 1.926 1.00 82.09 ATOM 24 CA ALA A 701 −47.958 24.364 0.957 1.00 81.38 ATOM 25 C ALA A 701 −47.697 23.318 −0.117 1.00 80.59 ATOM 26 O ALA A 701 −47.769 22.118 0.149 1.00 81.14 ATOM 27 CB ALA A 701 −46.646 24.755 1.643 1.00 81.49 ATOM 28 N GLY A 702 −47.399 23.766 −1.328 1.00 79.29 ATOM 29 CA GLY A 702 −47.139 22.814 −2.389 1.00 79.40 ATOM 30 C GLY A 702 −46.042 21.833 −2.016 1.00 78.74 ATOM 31 O GLY A 702 −46.226 20.612 −2.070 1.00 78.53 ATOM 32 N THR A 703 −44.902 22.387 −1.615 1.00 77.41 ATOM 33 CA THR A 703 −43.720 21.621 −1.238 1.00 75.67 ATOM 34 C THR A 703 −43.960 20.300 −0.510 1.00 73.00 ATOM 35 O THR A 703 −44.742 20.222 0.432 1.00 73.21 ATOM 36 CB THR A 703 −42.780 22.481 −0.378 1.00 77.78 ATOM 37 OG1 THR A 703 −42.497 23.708 −1.065 1.00 78.99 ATOM 38 CG2 THR A 703 −41.473 21.740 −0.108 1.00 78.77 ATOM 39 N ALA A 704 −43.259 19.264 −0.960 1.00 70.01 ATOM 40 CA ALA A 704 −43.361 17.942 −0.366 1.00 66.51 ATOM 41 C ALA A 704 −42.270 17.799 0.688 1.00 65.00 ATOM 42 O ALA A 704 −41.318 18.588 0.737 1.00 63.04 ATOM 43 CB ALA A 704 −43.201 16.872 −1.435 1.00 66.82 ATOM 44 N PRO A 705 −42.395 16.788 1.552 1.00 62.77 ATOM 45 CA PRO A 705 −41.399 16.577 2.597 1.00 61.58 ATOM 46 C PRO A 705 −40.009 16.258 2.067 1.00 60.23 ATOM 47 O PRO A 705 −39.843 15.521 1.095 1.00 61.36 ATOM 48 CB PRO A 705 −41.993 15.430 3.410 1.00 61.65 ATOM 49 CG PRO A 705 −42.736 14.656 2.391 1.00 63.07 ATOM 50 CD PRO A 705 −43.418 15.730 1.581 1.00 63.22 ATOM 51 N ASN A 706 −39.017 16.843 2.724 1.00 57.06 ATOM 52 CA ASN A 706 −37.621 16.649 2.392 1.00 54.07 ATOM 53 C ASN A 706 −37.112 15.494 3.264 1.00 53.97 ATOM 54 O ASN A 706 −36.701 15.707 4.404 1.00 52.73 ATOM 55 CB ASN A 706 −36.846 17.926 2.715 1.00 52.73 ATOM 56 CG ASN A 706 −35.377 17.816 2.374 1.00 52.89 ATOM 57 OD1 ASN A 706 −34.883 16.732 2.070 1.00 51.75 ATOM 58 ND2 ASN A 706 −34.664 18.940 2.434 1.00 51.00 ATOM 59 N GLN A 707 −37.137 14.274 2.740 1.00 51.97 ATOM 60 CA GLN A 707 −36.679 13.147 3.536 1.00 53.28 ATOM 61 C GLN A 707 −35.202 12.775 3.376 1.00 51.56 ATOM 62 O GLN A 707 −34.813 11.628 3.611 1.00 50.32 ATOM 63 CB GLN A 707 −37.563 11.925 3.280 1.00 52.48 ATOM 64 CG GLN A 707 −38.988 12.125 3.736 1.00 57.13 ATOM 65 CD GLN A 707 −39.850 10.906 3.491 1.00 60.12 ATOM 66 OE1 GLN A 707 −39.900 9.992 4.313 1.00 62.36 ATOM 67 NE2 GLN A 707 −40.523 10.876 2.338 1.00 60.48 ATOM 68 N ALA A 708 −34.378 13.742 2.990 1.00 49.29 ATOM 69 CA ALA A 708 −32.950 13.483 2.843 1.00 48.15 ATOM 70 C ALA A 708 −32.400 13.031 4.202 1.00 48.57 ATOM 71 O ALA A 708 −32.871 13.477 5.248 1.00 47.60 ATOM 72 CB ALA A 708 −32.239 14.741 2.390 1.00 45.11 ATOM 73 N GLN A 709 −31.416 12.138 4.187 1.00 49.32 ATOM 74 CA GLN A 709 −30.824 11.662 5.430 1.00 49.62 ATOM 75 C GLN A 709 −29.474 12.323 5.665 1.00 50.85 ATOM 76 O GLN A 709 −28.692 12.528 4.736 1.00 52.52 ATOM 77 CB GLN A 709 −30.627 10.145 5.388 1.00 48.60 ATOM 78 CG GLN A 709 −31.897 9.345 5.182 1.00 47.70 ATOM 79 CD GLN A 709 −32.848 9.427 6.353 1.00 47.21 ATOM 80 OE1 GLN A 709 −32.529 8.975 7.450 1.00 47.89 ATOM 81 NE2 GLN A 709 −34.027 10.004 6.126 1.00 44.74 ATOM 82 N LEU A 710 −29.212 12.668 6.913 1.00 51.76 ATOM 83 CA LEU A 710 −27.945 13.268 7.283 1.00 54.69 ATOM 84 C LEU A 710 −27.458 12.404 8.424 1.00 55.52 ATOM 85 O LEU A 710 −28.112 12.334 9.461 1.00 54.54 ATOM 86 CB LEU A 710 −28.129 14.702 7.782 1.00 56.03 ATOM 87 CG LEU A 710 −26.833 15.259 8.384 1.00 57.05 ATOM 88 CD1 LEU A 710 −25.863 15.544 7.264 1.00 56.49 ATOM 89 CD2 LEU A 710 −27.102 16.510 9.198 1.00 57.87 ATOM 90 N ARG A 711 −26.321 11.742 8.247 1.00 56.82 ATOM 91 CA ARG A 711 −25.821 10.877 9.302 1.00 58.00 ATOM 92 C ARG A 711 −24.737 11.545 10.114 1.00 56.44 ATOM 93 O ARG A 711 −23.756 12.036 9.577 1.00 55.70 ATOM 94 CB ARG A 711 −25.327 9.556 8.710 1.00 60.89 ATOM 95 CG ARG A 711 −26.351 8.925 7.763 1.00 67.44 ATOM 96 CD ARG A 711 −25.971 7.525 7.317 1.00 71.94 ATOM 97 NE ARG A 711 −26.098 6.561 8.406 1.00 76.65 ATOM 98 CZ ARG A 711 −25.853 5.258 8.283 1.00 78.71 ATOM 99 NH1 ARG A 711 −25.465 4.760 7.111 1.00 78.46 ATOM 100 NH2 ARG A 711 −26.002 4.455 9.331 1.00 78.34 ATOM 101 N ILE A 712 −24.946 11.584 11.422 1.00 57.82 ATOM 102 CA ILE A 712 −23.988 12.181 12.342 1.00 59.70 ATOM 103 C ILE A 712 −23.017 11.065 12.730 1.00 59.96 ATOM 104 O ILE A 712 −23.401 10.089 13.363 1.00 59.83 ATOM 105 CB ILE A 712 −24.727 12.748 13.562 1.00 59.41 ATOM 106 CG1 ILE A 712 −25.841 13.673 13.057 1.00 60.67 ATOM 107 CG2 ILE A 712 −23.760 13.512 14.469 1.00 57.78 ATOM 108 CD1 ILE A 712 −26.793 14.166 14.119 1.00 62.84 ATOM 109 N LEU A 713 −21.761 11.215 12.328 1.00 60.81 ATOM 110 CA LEU A 713 −20.753 10.191 12.566 1.00 62.74 ATOM 111 C LEU A 713 −19.812 10.411 13.736 1.00 63.70 ATOM 112 O LEU A 713 −19.297 11.512 13.939 1.00 63.91 ATOM 113 CB LEU A 713 −19.907 10.007 11.307 1.00 62.56 ATOM 114 CG LEU A 713 −20.661 9.698 10.016 1.00 62.99 ATOM 115 CD1 LEU A 713 −19.656 9.255 8.970 1.00 64.29 ATOM 116 CD2 LEU A 713 −21.714 8.620 10.254 1.00 62.63 ATOM 117 N ALA A 714 −19.581 9.343 14.494 1.00 64.16 ATOM 118 CA ALA A 714 −18.669 9.405 15.618 1.00 64.73 ATOM 119 C ALA A 714 −17.294 9.443 14.978 1.00 65.80 ATOM 120 O ALA A 714 −17.011 8.687 14.047 1.00 65.21 ATOM 121 CB ALA A 714 −18.816 8.168 16.494 1.00 65.59 ATOM 122 N GLU A 715 −16.461 10.352 15.470 1.00 67.13 ATOM 123 CA GLU A 715 −15.092 10.556 15.000 1.00 68.35 ATOM 124 C GLU A 715 −14.346 9.234 14.778 1.00 68.80 ATOM 125 O GLU A 715 −13.419 9.145 13.965 1.00 67.36 ATOM 126 CB GLU A 715 −14.370 11.404 16.046 1.00 70.35 ATOM 127 CG GLU A 715 −12.937 11.784 15.762 1.00 74.38 ATOM 128 CD GLU A 715 −12.337 12.568 16.925 1.00 76.58 ATOM 129 OE1 GLU A 715 −11.155 12.966 16.837 1.00 79.37 ATOM 130 OE2 GLU A 715 −13.051 12.785 17.932 1.00 75.16 ATOM 131 N THR A 716 −14.779 8.211 15.509 1.00 68.91 ATOM 132 CA THR A 716 −14.189 6.880 15.465 1.00 68.54 ATOM 133 C THR A 716 −14.486 6.062 14.214 1.00 67.91 ATOM 134 O THR A 716 −13.757 5.117 13.901 1.00 67.89 ATOM 135 CB THR A 716 −14.643 6.049 16.675 1.00 69.38 ATOM 136 OG1 THR A 716 −14.187 4.700 16.521 1.00 72.15 ATOM 137 CG2 THR A 716 −16.163 6.049 16.782 1.00 69.99 ATOM 138 N GLU A 717 −15.551 6.408 13.500 1.00 66.43 ATOM 139 CA GLU A 717 −15.910 5.661 12.302 1.00 65.47 ATOM 140 C GLU A 717 −15.111 6.104 11.085 1.00 64.70 ATOM 141 O GLU A 717 −15.137 5.440 10.047 1.00 63.74 ATOM 142 CB GLU A 717 −17.408 5.806 12.035 1.00 65.65 ATOM 143 CG GLU A 717 −18.276 5.259 13.166 1.00 65.53 ATOM 144 CD GLU A 717 −19.658 5.892 13.215 1.00 65.95 ATOM 145 OE1 GLU A 717 −20.471 5.662 12.291 1.00 62.49 ATOM 146 OE2 GLU A 717 −19.922 6.635 14.187 1.00 67.09 ATOM 147 N LEU A 718 −14.382 7.211 11.223 1.00 64.90 ATOM 148 CA LEU A 718 −13.591 7.752 10.119 1.00 65.63 ATOM 149 C LEU A 718 −12.082 7.598 10.274 1.00 67.11 ATOM 150 O LEU A 718 −11.521 7.846 11.345 1.00 66.91 ATOM 151 CB LEU A 718 −13.909 9.236 9.917 1.00 64.23 ATOM 152 CG LEU A 718 −15.353 9.609 9.575 1.00 64.11 ATOM 153 CD1 LEU A 718 −15.478 11.119 9.521 1.00 63.98 ATOM 154 CD2 LEU A 718 −15.757 8.988 8.251 1.00 62.29 ATOM 155 N ALA A 719 −11.435 7.204 9.178 1.00 67.97 ATOM 156 CA ALA A 719 −9.986 7.027 9.139 1.00 67.89 ATOM 157 C ALA A 719 −9.394 7.806 7.968 1.00 67.48 ATOM 158 O ALA A 719 −9.687 7.518 6.805 1.00 67.27 ATOM 159 CB ALA A 719 −9.634 5.544 9.004 1.00 66.89 ATOM 160 N ARG A 720 −8.572 8.801 8.284 1.00 67.63 ATOM 161 CA ARG A 720 −7.918 9.605 7.264 1.00 67.22 ATOM 162 C ARG A 720 −6.859 8.725 6.599 1.00 69.63 ATOM 163 O ARG A 720 −6.763 7.534 6.890 1.00 70.38 ATOM 164 CB ARG A 720 −7.230 10.810 7.901 1.00 65.71 ATOM 165 CG ARG A 720 −8.103 11.668 8.793 1.00 65.13 ATOM 166 CD ARG A 720 −7.881 13.135 8.465 1.00 65.92 ATOM 167 NE ARG A 720 −8.268 14.063 9.529 1.00 67.39 ATOM 168 CZ ARG A 720 −9.421 14.033 10.197 1.00 70.61 ATOM 169 NH1 ARG A 720 −10.342 13.103 9.939 1.00 70.23 ATOM 170 NH2 ARG A 720 −9.670 14.966 11.112 1.00 70.99 ATOM 171 N VAL A 721 −6.060 9.315 5.716 1.00 71.34 ATOM 172 CA VAL A 721 −4.988 8.599 5.018 1.00 71.66 ATOM 173 C VAL A 721 −3.988 9.622 4.478 1.00 73.14 ATOM 174 O VAL A 721 −3.027 10.001 5.157 1.00 73.20 ATOM 175 CB VAL A 721 −5.533 7.764 3.833 1.00 70.82 ATOM 176 CG1 VAL A 721 −4.386 7.253 2.984 1.00 70.96 ATOM 177 CG2 VAL A 721 −6.344 6.592 4.347 1.00 70.37 ATOM 178 N ALA A 722 −4.225 10.063 3.249 1.00 73.97 ATOM 179 CA ALA A 722 −3.381 11.060 2.611 1.00 73.28 ATOM 180 C ALA A 722 −4.262 12.283 2.405 1.00 72.83 ATOM 181 O ALA A 722 −5.476 12.231 2.627 1.00 73.18 ATOM 182 CB ALA A 722 −2.873 10.545 1.262 1.00 72.83 ATOM 183 N VAL A 723 −3.640 13.381 1.996 1.00 71.49 ATOM 184 CA VAL A 723 −4.356 14.615 1.728 1.00 68.53 ATOM 185 C VAL A 723 −4.620 14.680 0.231 1.00 68.55 ATOM 186 O VAL A 723 −3.765 14.319 −0.576 1.00 67.71 ATOM 187 CB VAL A 723 −3.527 15.842 2.138 1.00 67.22 ATOM 188 CG1 VAL A 723 −4.174 17.111 1.605 1.00 66.63 ATOM 189 CG2 VAL A 723 −3.410 15.900 3.649 1.00 66.06 ATOM 190 N LEU A 724 −5.815 15.120 −0.138 1.00 68.80 ATOM 191 CA LEU A 724 −6.164 15.243 −1.542 1.00 68.52 ATOM 192 C LEU A 724 −5.904 16.689 −1.969 1.00 69.72 ATOM 193 O LEU A 724 −5.843 17.008 −3.156 1.00 71.11 ATOM 194 CB LEU A 724 −7.630 14.859 −1.739 1.00 66.79 ATOM 195 CG LEU A 724 −7.933 13.385 −1.456 1.00 65.65 ATOM 196 CD1 LEU A 724 −9.426 13.156 −1.423 1.00 65.45 ATOM 197 CD2 LEU A 724 −7.287 12.516 −2.526 1.00 66.07 ATOM 198 N GLY A 725 −5.721 17.554 −0.979 1.00 70.85 ATOM 199 CA GLY A 725 −5.467 18.954 −1.244 1.00 72.13 ATOM 200 C GLY A 725 −6.098 19.804 −0.160 1.00 73.79 ATOM 201 O GLY A 725 −6.806 19.290 0.707 1.00 73.67 ATOM 202 N SER A 726 −5.842 21.106 −0.204 1.00 75.09 ATOM 203 CA SER A 726 −6.400 22.022 0.780 1.00 76.38 ATOM 204 C SER A 726 −6.234 23.459 0.316 1.00 76.97 ATOM 205 O SER A 726 −5.127 23.899 0.005 1.00 77.58 ATOM 206 CB SER A 726 −5.707 21.846 2.133 1.00 77.43 ATOM 207 OG SER A 726 −4.369 22.314 2.090 1.00 77.62 ATOM 208 N GLY A 727 −7.346 24.183 0.265 1.00 77.88 ATOM 209 CA GLY A 727 −7.309 25.570 −0.151 1.00 77.49 ATOM 210 C GLY A 727 −7.857 26.428 0.962 1.00 77.71 ATOM 211 O GLY A 727 −7.950 25.984 2.107 1.00 76.78 ATOM 212 N ALA A 728 −8.222 27.658 0.633 1.00 78.59 ATOM 213 CA ALA A 728 −8.772 28.569 1.623 1.00 79.53 ATOM 214 C ALA A 728 −10.094 28.003 2.130 1.00 80.29 ATOM 215 O ALA A 728 −10.689 28.515 3.081 1.00 80.59 ATOM 216 CB ALA A 728 −8.991 29.934 0.999 1.00 80.42 ATOM 217 N PHE A 729 −10.533 26.924 1.495 1.00 80.52 ATOM 218 CA PHE A 729 −11.789 26.283 1.845 1.00 80.77 ATOM 219 C PHE A 729 −11.635 25.114 2.815 1.00 80.36 ATOM 220 O PHE A 729 −12.611 24.430 3.122 1.00 81.24 ATOM 221 CB PHE A 729 −12.480 25.821 0.563 1.00 81.06 ATOM 222 CG PHE A 729 −12.521 26.879 −0.503 1.00 82.69 ATOM 223 CD1 PHE A 729 −11.372 27.197 −1.230 1.00 83.00 ATOM 224 CD2 PHE A 729 −13.690 27.601 −0.744 1.00 82.96 ATOM 225 CE1 PHE A 729 −11.385 28.222 −2.180 1.00 82.28 ATOM 226 CE2 PHE A 729 −13.712 28.625 −1.690 1.00 82.16 ATOM 227 CZ PHE A 729 −12.555 28.936 −2.408 1.00 81.83 ATOM 228 N GLY A 730 −10.417 24.895 3.307 1.00 78.97 ATOM 229 CA GLY A 730 −10.176 23.800 4.234 1.00 75.86 ATOM 230 C GLY A 730 −9.385 22.674 3.591 1.00 74.02 ATOM 231 O GLY A 730 −9.022 22.756 2.418 1.00 74.18 ATOM 232 N THR A 731 −9.124 21.613 4.347 1.00 71.57 ATOM 233 CA THR A 731 −8.366 20.489 3.821 1.00 69.93 ATOM 234 C THR A 731 −9.233 19.271 3.521 1.00 69.30 ATOM 235 O THR A 731 −10.110 18.911 4.310 1.00 68.76 ATOM 236 CB THR A 731 −7.255 20.078 4.795 1.00 70.50 ATOM 237 OG1 THR A 731 −6.360 21.180 4.985 1.00 69.99 ATOM 238 CG2 THR A 731 −6.479 18.893 4.244 1.00 69.46 ATOM 239 N VAL A 732 −8.971 18.639 2.378 1.00 68.82 ATOM 240 CA VAL A 732 −9.720 17.462 1.944 1.00 69.33 ATOM 241 C VAL A 732 −8.852 16.202 1.933 1.00 70.00 ATOM 242 O VAL A 732 −7.975 16.057 1.087 1.00 70.94 ATOM 243 CB VAL A 732 −10.299 17.658 0.517 1.00 69.44 ATOM 244 CG1 VAL A 732 −11.149 16.457 0.143 1.00 69.31 ATOM 245 CG2 VAL A 732 −11.123 18.942 0.439 1.00 67.78 ATOM 246 N TYR A 733 −9.112 15.291 2.867 1.00 70.94 ATOM 247 CA TYR A 733 −8.361 14.040 2.980 1.00 70.76 ATOM 248 C TYR A 733 −9.094 12.875 2.331 1.00 71.20 ATOM 249 O TYR A 733 −10.322 12.862 2.263 1.00 70.51 ATOM 250 CB TYR A 733 −8.164 13.661 4.449 1.00 73.12 ATOM 251 CG TYR A 733 −7.466 14.679 5.318 1.00 75.05 ATOM 252 CD1 TYR A 733 −6.080 14.646 5.498 1.00 75.57 ATOM 253 CD2 TYR A 733 −8.193 15.665 5.984 1.00 75.38 ATOM 254 CE1 TYR A 733 −5.439 15.571 6.326 1.00 74.72 ATOM 255 CE2 TYR A 733 −7.564 16.594 6.809 1.00 75.15 ATOM 256 CZ TYR A 733 −6.191 16.541 6.973 1.00 75.27 ATOM 257 OH TYR A 733 −5.578 17.472 7.774 1.00 77.22 ATOM 258 N LYS A 734 −8.340 11.888 1.857 1.00 72.36 ATOM 259 CA LYS A 734 −8.955 10.688 1.294 1.00 72.08 ATOM 260 C LYS A 734 −9.168 9.821 2.534 1.00 71.34 ATOM 261 O LYS A 734 −8.445 9.984 3.524 1.00 69.91 ATOM 262 CB LYS A 734 −8.005 9.974 0.333 1.00 72.27 ATOM 263 CG LYS A 734 −8.519 8.605 −0.097 1.00 73.95 ATOM 264 CD LYS A 734 −7.471 7.804 −0.857 1.00 73.38 ATOM 265 CE LYS A 734 −7.982 6.400 −1.146 1.00 73.91 ATOM 266 NZ LYS A 734 −7.047 5.599 −1.976 1.00 72.92 ATOM 267 N GLY A 735 −10.139 8.913 2.512 1.00 70.61 ATOM 268 CA GLY A 735 −10.338 8.104 3.702 1.00 71.08 ATOM 269 C GLY A 735 −11.390 7.015 3.719 1.00 71.04 ATOM 270 O GLY A 735 −12.152 6.839 2.767 1.00 71.51 ATOM 271 N ILE A 736 −11.422 6.281 4.829 1.00 71.26 ATOM 272 CA ILE A 736 −12.368 5.188 5.005 1.00 72.22 ATOM 273 C ILE A 736 −13.364 5.496 6.107 1.00 72.21 ATOM 274 O ILE A 736 −13.003 6.023 7.161 1.00 71.05 ATOM 275 CB ILE A 736 −11.673 3.867 5.415 1.00 73.36 ATOM 276 CG1 ILE A 736 −10.379 3.663 4.621 1.00 74.33 ATOM 277 CG2 ILE A 736 −12.627 2.698 5.186 1.00 71.11 ATOM 278 CD1 ILE A 736 −9.552 2.470 5.102 1.00 75.22 ATOM 279 N TRP A 737 −14.618 5.146 5.858 1.00 72.87 ATOM 280 CA TRP A 737 −15.674 5.346 6.832 1.00 73.66 ATOM 281 C TRP A 737 −16.373 4.014 7.085 1.00 75.42 ATOM 282 O TRP A 737 −16.835 3.358 6.147 1.00 75.21 ATOM 283 CB TRP A 737 −16.681 6.383 6.328 1.00 71.21 ATOM 284 CG TRP A 737 −17.960 6.395 7.106 1.00 69.09 ATOM 285 CD1 TRP A 737 −18.096 6.373 8.466 1.00 68.36 ATOM 286 CD2 TRP A 737 −19.285 6.432 6.571 1.00 68.26 ATOM 287 NE1 TRP A 737 −19.426 6.391 8.810 1.00 67.91 ATOM 288 CE2 TRP A 737 −20.179 6.430 7.668 1.00 67.63 ATOM 289 CE3 TRP A 737 −19.806 6.470 5.271 1.00 67.83 ATOM 290 CZ2 TRP A 737 −21.565 6.463 7.506 1.00 67.13 ATOM 291 CZ3 TRP A 737 −21.189 6.503 5.107 1.00 68.96 ATOM 292 CH2 TRP A 737 −22.053 6.500 6.223 1.00 68.91 ATOM 293 N VAL A 738 −16.437 3.619 8.355 1.00 76.80 ATOM 294 CA VAL A 738 −17.085 2.374 8.746 1.00 78.00 ATOM 295 C VAL A 738 −18.328 2.714 9.563 1.00 79.76 ATOM 296 O VAL A 738 −18.226 3.062 10.736 1.00 80.23 ATOM 297 CB VAL A 738 −16.146 1.511 9.600 1.00 78.37 ATOM 298 CG1 VAL A 738 −16.738 0.125 9.772 1.00 77.43 ATOM 299 CG2 VAL A 738 −14.761 1.446 8.957 1.00 77.28 ATOM 300 N PRO A 739 −19.518 2.605 8.948 1.00 81.79 ATOM 301 CA PRO A 739 −20.837 2.887 9.531 1.00 83.53 ATOM 302 C PRO A 739 −21.013 2.624 11.025 1.00 85.81 ATOM 303 O PRO A 739 −20.216 1.912 11.643 1.00 85.32 ATOM 304 CB PRO A 739 −21.768 2.042 8.676 1.00 82.99 ATOM 305 CG PRO A 739 −21.149 2.186 7.327 1.00 83.21 ATOM 306 CD PRO A 739 −19.671 1.980 7.621 1.00 82.26 ATOM 307 N ALA A 740 −22.076 3.207 11.585 1.00 87.67 ATOM 308 CA ALA A 740 −22.407 3.091 13.008 1.00 89.23 ATOM 309 C ALA A 740 −22.747 1.670 13.453 1.00 90.19 ATOM 310 O ALA A 740 −23.730 1.456 14.170 1.00 90.44 ATOM 311 CB ALA A 740 −23.571 4.031 13.345 1.00 88.58 ATOM 312 N GLY A 741 −21.929 0.708 13.034 1.00 90.71 ATOM 313 CA GLY A 741 −22.156 −0.680 13.396 1.00 91.14 ATOM 314 C GLY A 741 −22.167 −1.612 12.199 1.00 91.59 ATOM 315 O GLY A 741 −23.100 −2.396 12.025 1.00 91.52 ATOM 316 N GLU A 742 −21.130 −1.528 11.369 1.00 91.74 ATOM 317 CA GLU A 742 −21.033 −2.374 10.185 1.00 91.44 ATOM 318 C GLU A 742 −19.579 −2.705 9.875 1.00 91.13 ATOM 319 O GLU A 742 −18.667 −2.139 10.475 1.00 90.38 ATOM 320 CB GLU A 742 −21.688 −1.680 8.986 1.00 91.24 ATOM 321 CG GLU A 742 −23.106 −1.209 9.276 1.00 91.68 ATOM 322 CD GLU A 742 −23.905 −0.905 8.027 1.00 92.00 ATOM 323 OE1 GLU A 742 −23.483 −0.040 7.232 1.00 91.88 ATOM 324 OE2 GLU A 742 −24.966 −1.538 7.844 1.00 91.68 ATOM 325 N ALA A 743 −19.370 −3.625 8.936 1.00 91.28 ATOM 326 CA ALA A 743 −18.024 −4.048 8.559 1.00 91.22 ATOM 327 C ALA A 743 −17.472 −3.312 7.335 1.00 91.06 ATOM 328 O ALA A 743 −16.276 −3.011 7.273 1.00 90.46 ATOM 329 CB ALA A 743 −18.010 −5.559 8.307 1.00 90.34 ATOM 330 N VAL A 744 −18.346 −3.025 6.371 1.00 90.80 ATOM 331 CA VAL A 744 −17.950 −2.344 5.135 1.00 89.78 ATOM 332 C VAL A 744 −17.025 −1.146 5.353 1.00 88.68 ATOM 333 O VAL A 744 −17.191 −0.380 6.301 1.00 89.33 ATOM 334 CB VAL A 744 −19.191 −1.867 4.323 1.00 89.22 ATOM 335 CG1 VAL A 744 −20.073 −3.053 3.983 1.00 89.59 ATOM 336 CG2 VAL A 744 −19.975 −0.831 5.111 1.00 88.82 ATOM 337 N LYS A 745 −16.042 −0.999 4.469 1.00 86.57 ATOM 338 CA LYS A 745 −15.098 0.111 4.542 1.00 84.05 ATOM 339 C LYS A 745 −15.364 1.094 3.401 1.00 82.42 ATOM 340 O LYS A 745 −14.580 1.174 2.460 1.00 81.96 ATOM 341 CB LYS A 745 −13.655 −0.399 4.439 1.00 83.71 ATOM 342 CG LYS A 745 −13.093 −1.055 5.696 1.00 82.67 ATOM 343 CD LYS A 745 −11.580 −1.229 5.574 1.00 81.20 ATOM 344 CE LYS A 745 −10.962 −1.742 6.864 1.00 81.60 ATOM 345 NZ LYS A 745 −9.473 −1.807 6.792 1.00 80.27 ATOM 346 N ILE A 746 −16.469 1.834 3.486 1.00 80.20 ATOM 347 CA ILE A 746 −16.829 2.804 2.451 1.00 77.59 ATOM 348 C ILE A 746 −15.753 3.867 2.234 1.00 75.28 ATOM 349 O ILE A 746 −15.354 4.565 3.165 1.00 75.06 ATOM 350 CB ILE A 746 −18.153 3.521 2.784 1.00 78.03 ATOM 351 CG1 ILE A 746 −19.299 2.508 2.844 1.00 78.83 ATOM 352 CG2 ILE A 746 −18.451 4.568 1.726 1.00 79.05 ATOM 353 CD1 ILE A 746 −20.671 3.125 3.096 1.00 78.81 ATOM 354 N PRO A 747 −15.268 4.000 0.990 1.00 74.01 ATOM 355 CA PRO A 747 −14.235 4.985 0.654 1.00 71.83 ATOM 356 C PRO A 747 −14.866 6.370 0.601 1.00 70.14 ATOM 357 O PRO A 747 −15.882 6.574 −0.077 1.00 68.69 ATOM 358 CB PRO A 747 −13.753 4.510 −0.709 1.00 71.63 ATOM 359 CG PRO A 747 −15.018 4.016 −1.336 1.00 72.44 ATOM 360 CD PRO A 747 −15.673 3.237 −0.207 1.00 74.00 ATOM 361 N VAL A 748 −14.269 7.322 1.311 1.00 67.54 ATOM 362 CA VAL A 748 −14.820 8.669 1.346 1.00 65.96 ATOM 363 C VAL A 748 −13.797 9.791 1.302 1.00 64.98 ATOM 364 O VAL A 748 −12.584 9.565 1.370 1.00 63.82 ATOM 365 CB VAL A 748 −15.659 8.902 2.622 1.00 66.10 ATOM 366 CG1 VAL A 748 −16.839 7.953 2.666 1.00 65.30 ATOM 367 CG2 VAL A 748 −14.776 8.731 3.846 1.00 64.29 ATOM 368 N ALA A 749 −14.325 11.008 1.179 1.00 62.57 ATOM 369 CA ALA A 749 −13.525 12.221 1.172 1.00 61.68 ATOM 370 C ALA A 749 −14.004 12.942 2.411 1.00 61.42 ATOM 371 O ALA A 749 −15.204 13.026 2.656 1.00 62.73 ATOM 372 CB ALA A 749 −13.814 13.058 0.060 1.00 60.54 ATOM 373 N ILE A 750 −13.070 13.432 3.212 1.00 60.76 ATOM 374 CA ILE A 750 −13.425 14.143 4.423 1.00 59.53 ATOM 375 C ILE A 750 −12.830 15.519 4.312 1.00 58.84 ATOM 376 O ILE A 750 −11.650 15.667 4.014 1.00 58.42 ATOM 377 CB ILE A 750 −12.855 13.456 5.671 1.00 59.88 ATOM 378 CG1 ILE A 750 −13.315 11.999 5.710 1.00 61.77 ATOM 379 CG2 ILE A 750 −13.312 14.193 6.917 1.00 59.44 ATOM 380 CD1 ILE A 750 −12.707 11.180 6.836 1.00 64.53 ATOM 381 N LYS A 751 −13.654 16.529 4.532 1.00 59.29 ATOM 382 CA LYS A 751 −13.188 17.897 4.458 1.00 60.16 ATOM 383 C LYS A 751 −13.373 18.529 5.814 1.00 61.42 ATOM 384 O LYS A 751 −14.406 18.347 6.463 1.00 60.51 ATOM 385 CB LYS A 751 −13.982 18.676 3.410 1.00 59.82 ATOM 386 CG LYS A 751 −13.519 20.109 3.247 1.00 59.02 ATOM 387 CD LYS A 751 −14.138 20.745 2.021 1.00 58.49 ATOM 388 CE LYS A 751 −13.435 22.035 1.690 1.00 57.20 ATOM 389 NZ LYS A 751 −13.915 22.606 0.411 1.00 58.47 ATOM 390 N ILE A 752 −12.365 19.271 6.242 1.00 63.64 ATOM 391 CA ILE A 752 −12.420 19.935 7.528 1.00 66.22 ATOM 392 C ILE A 752 −12.349 21.438 7.329 1.00 67.39 ATOM 393 O ILE A 752 −11.394 21.945 6.749 1.00 67.55 ATOM 394 CB ILE A 752 −11.256 19.473 8.422 1.00 66.68 ATOM 395 CG1 ILE A 752 −11.241 17.943 8.481 1.00 66.85 ATOM 396 CG2 ILE A 752 −11.404 20.065 9.818 1.00 67.28 ATOM 397 CD1 ILE A 752 −10.147 17.356 9.336 1.00 66.47 ATOM 398 N ALA A 753 −13.372 22.146 7.799 1.00 70.53 ATOM 399 CA ALA A 753 −13.419 23.602 7.673 1.00 74.64 ATOM 400 C ALA A 753 −12.365 24.214 8.594 1.00 76.96 ATOM 401 O ALA A 753 −11.877 23.534 9.500 1.00 77.82 ATOM 402 CB ALA A 753 −14.806 24.110 8.038 1.00 73.77 ATOM 403 N VAL A 754 −12.020 25.485 8.372 1.00 79.45 ATOM 404 CA VAL A 754 −10.997 26.157 9.189 1.00 81.01 ATOM 405 CB VAL A 754 −10.273 27.279 8.378 1.00 80.88 ATOM 406 CG1 VAL A 754 −8.977 27.694 9.096 1.00 78.71 ATOM 407 CG2 VAL A 754 −9.989 26.799 6.945 1.00 79.23 ATOM 408 C VAL A 754 −11.541 26.769 10.494 1.00 82.00 ATOM 409 OT1 VAL A 754 −11.212 27.942 10.798 1.00 82.05 ATOM 410 OT2 VAL A 754 −12.277 26.057 11.216 1.00 82.11 ATOM 411 N ALA A 761 −22.557 30.871 14.717 1.00 87.31 ATOM 412 CA ALA A 761 −22.100 30.438 13.364 1.00 87.94 ATOM 413 C ALA A 761 −22.469 28.982 13.071 1.00 88.76 ATOM 414 O ALA A 761 −23.035 28.682 12.017 1.00 89.19 ATOM 415 CB ALA A 761 −20.589 30.632 13.236 1.00 86.83 ATOM 416 N ASN A 762 −22.147 28.080 13.995 1.00 88.98 ATOM 417 CA ASN A 762 −22.459 26.666 13.812 1.00 89.06 ATOM 418 C ASN A 762 −23.933 26.471 13.493 1.00 89.09 ATOM 419 O ASN A 762 −24.339 25.428 12.975 1.00 89.26 ATOM 420 CB ASN A 762 −22.083 25.865 15.060 1.00 89.85 ATOM 421 CG ASN A 762 −20.608 25.519 15.102 1.00 90.47 ATOM 422 OD1 ASN A 762 −19.749 26.403 15.132 1.00 89.73 ATOM 423 ND2 ASN A 762 −20.306 24.225 15.098 1.00 90.01 ATOM 424 N VAL A 763 −24.735 27.481 13.811 1.00 88.96 ATOM 425 CA VAL A 763 −26.160 27.425 13.533 1.00 88.35 ATOM 426 C VAL A 763 −26.274 27.447 12.020 1.00 88.39 ATOM 427 O VAL A 763 −26.950 26.609 11.427 1.00 88.27 ATOM 428 CB VAL A 763 −26.899 28.657 14.076 1.00 88.18 ATOM 429 CG1 VAL A 763 −28.380 28.348 14.200 1.00 87.36 ATOM 430 CG2 VAL A 763 −26.302 29.086 15.406 1.00 88.46 ATOM 431 N GLU A 764 −25.598 28.420 11.408 1.00 87.88 ATOM 432 CA GLU A 764 −25.599 28.574 9.956 1.00 86.88 ATOM 433 C GLU A 764 −25.164 27.260 9.339 1.00 84.91 ATOM 434 O GLU A 764 −25.826 26.724 8.448 1.00 85.31 ATOM 435 CB GLU A 764 −24.609 29.654 9.507 1.00 88.52 ATOM 436 CG GLU A 764 −24.708 30.982 10.231 1.00 90.41 ATOM 437 CD GLU A 764 −23.821 32.047 9.600 1.00 91.24 ATOM 438 OE1 GLU A 764 −22.685 31.714 9.190 1.00 92.50 ATOM 439 OE2 GLU A 764 −24.254 33.218 9.523 1.00 91.08 ATOM 440 N PHE A 765 −24.037 26.751 9.823 1.00 81.83 ATOM 441 CA PHE A 765 −23.491 25.507 9.322 1.00 78.37 ATOM 442 C PHE A 765 −24.495 24.367 9.297 1.00 75.51 ATOM 443 O PHE A 765 −24.687 23.722 8.269 1.00 74.23 ATOM 444 CB PHE A 765 −22.280 25.080 10.141 1.00 79.06 ATOM 445 CG PHE A 765 −21.729 23.762 9.717 1.00 80.47 ATOM 446 CD1 PHE A 765 −22.371 22.577 10.079 1.00 81.96 ATOM 447 CD2 PHE A 765 −20.638 23.701 8.861 1.00 80.75 ATOM 448 CE1 PHE A 765 −21.945 21.353 9.586 1.00 81.90 ATOM 449 CE2 PHE A 765 −20.201 22.482 8.360 1.00 82.39 ATOM 450 CZ PHE A 765 −20.861 21.302 8.722 1.00 82.56 ATOM 451 N MET A 766 −25.117 24.092 10.433 1.00 72.71 ATOM 452 CA MET A 766 −26.083 23.014 10.472 1.00 70.93 ATOM 453 C MET A 766 −27.205 23.255 9.468 1.00 69.55 ATOM 454 O MET A 766 −27.946 22.338 9.120 1.00 70.42 ATOM 455 CB MET A 766 −26.638 22.849 11.887 1.00 71.33 ATOM 456 CG MET A 766 −25.603 22.336 12.873 1.00 71.61 ATOM 457 SD MET A 766 −24.622 20.959 12.199 1.00 74.04 ATOM 458 CE MET A 766 −25.720 19.631 12.348 1.00 69.51 ATOM 459 N ASP A 767 −27.331 24.489 8.995 1.00 66.54 ATOM 460 CA ASP A 767 −28.355 24.795 8.011 1.00 65.26 ATOM 461 C ASP A 767 −27.783 24.538 6.629 1.00 63.58 ATOM 462 O ASP A 767 −28.415 23.896 5.795 1.00 64.00 ATOM 463 CB ASP A 767 −28.807 26.249 8.131 1.00 67.20 ATOM 464 CG ASP A 767 −29.615 26.504 9.390 1.00 68.51 ATOM 465 OD1 ASP A 767 −30.624 25.794 9.594 1.00 68.20 ATOM 466 OD2 ASP A 767 −29.242 27.408 10.172 1.00 68.59 ATOM 467 N GLU A 768 −26.577 25.034 6.395 1.00 61.36 ATOM 468 CA GLU A 768 −25.917 24.841 5.118 1.00 60.21 ATOM 469 C GLU A 768 −25.744 23.350 4.846 1.00 58.77 ATOM 470 O GLU A 768 −25.834 22.908 3.704 1.00 58.90 ATOM 471 CB GLU A 768 −24.555 25.531 5.123 1.00 62.67 ATOM 472 CG GLU A 768 −23.938 25.709 3.745 1.00 68.86 ATOM 473 CD GLU A 768 −24.809 26.548 2.806 1.00 72.06 ATOM 474 OE1 GLU A 768 −24.346 26.888 1.696 1.00 75.67 ATOM 475 OE2 GLU A 768 −25.960 26.866 3.168 1.00 73.63 ATOM 476 N ALA A 769 −25.515 22.574 5.902 1.00 56.78 ATOM 477 CA ALA A 769 −25.329 21.134 5.764 1.00 53.94 ATOM 478 C ALA A 769 −26.602 20.437 5.328 1.00 53.30 ATOM 479 O ALA A 769 −26.547 19.423 4.626 1.00 55.21 ATOM 480 CB ALA A 769 −24.840 20.544 7.065 1.00 53.65 ATOM 481 N LEU A 770 −27.749 20.963 5.751 1.00 51.12 ATOM 482 CA LEU A 770 −29.029 20.373 5.370 1.00 50.39 ATOM 483 C LEU A 770 −29.127 20.440 3.851 1.00 49.87 ATOM 484 O LEU A 770 −29.584 19.502 3.194 1.00 48.92 ATOM 485 CB LEU A 770 −30.206 21.136 6.019 1.00 49.49 ATOM 486 CG LEU A 770 −31.615 20.629 5.648 1.00 50.99 ATOM 487 CD1 LEU A 770 −32.640 20.997 6.711 1.00 51.18 ATOM 488 CD2 LEU A 770 −32.026 21.204 4.295 1.00 48.88 ATOM 489 N ILE A 771 −28.683 21.561 3.298 1.00 49.87 ATOM 490 CA ILE A 771 −28.714 21.751 1.860 1.00 50.49 ATOM 491 C ILE A 771 −27.728 20.805 1.175 1.00 50.51 ATOM 492 O ILE A 771 −28.092 20.059 0.271 1.00 51.88 ATOM 493 CB ILE A 771 −28.352 23.196 1.491 1.00 49.76 ATOM 494 CG1 ILE A 771 −29.258 24.175 2.249 1.00 51.25 ATOM 495 CG2 ILE A 771 −28.509 23.394 −0.006 1.00 48.11 ATOM 496 CD1 ILE A 771 −30.729 24.104 1.846 1.00 52.39 ATOM 497 N MET A 772 −26.479 20.830 1.616 1.00 49.68 ATOM 498 CA MET A 772 −25.469 19.976 1.023 1.00 49.48 ATOM 499 C MET A 772 −25.925 18.544 1.041 1.00 49.90 ATOM 500 O MET A 772 −25.504 17.748 0.216 1.00 53.68 ATOM 501 CB MET A 772 −24.152 20.078 1.784 1.00 50.02 ATOM 502 CG MET A 772 −23.670 21.485 1.974 1.00 50.14 ATOM 503 SD MET A 772 −22.079 21.532 2.743 1.00 51.82 ATOM 504 CE MET A 772 −21.416 23.034 1.966 1.00 54.26 ATOM 505 N ALA A 773 −26.797 18.210 1.975 1.00 49.25 ATOM 506 CA ALA A 773 −27.265 16.841 2.078 1.00 49.85 ATOM 507 C ALA A 773 −28.569 16.559 1.339 1.00 49.63 ATOM 508 O ALA A 773 −28.963 15.405 1.189 1.00 49.98 ATOM 509 CB ALA A 773 −27.403 16.467 3.554 1.00 50.21 ATOM 510 N SER A 774 −29.243 17.597 0.867 1.00 50.09 ATOM 511 CA SER A 774 −30.507 17.385 0.172 1.00 51.17 ATOM 512 C SER A 774 −30.366 17.304 −1.333 1.00 50.49 ATOM 513 O SER A 774 −31.325 16.996 −2.027 1.00 53.51 ATOM 514 CB SER A 774 −31.503 18.496 0.514 1.00 50.00 ATOM 515 OG SER A 774 −31.733 18.568 1.903 1.00 53.58 ATOM 516 N MET A 775 −29.181 17.578 −1.850 1.00 51.19 ATOM 517 CA MET A 775 −28.991 17.536 −3.296 1.00 51.57 ATOM 518 C MET A 775 −29.005 16.115 −3.879 1.00 50.46 ATOM 519 O MET A 775 −28.128 15.298 −3.603 1.00 49.82 ATOM 520 CB MET A 775 −27.701 18.277 −3.657 1.00 52.20 ATOM 521 CG MET A 775 −27.711 19.720 −3.185 1.00 52.73 ATOM 522 SD MET A 775 −29.349 20.470 −3.403 1.00 58.26 ATOM 523 CE MET A 775 −29.044 21.567 −4.684 1.00 55.94 ATOM 524 N ASP A 776 −30.022 15.836 −4.688 1.00 49.69 ATOM 525 CA ASP A 776 −30.190 14.532 −5.309 1.00 47.92 ATOM 526 C ASP A 776 −30.278 14.653 −6.819 1.00 46.24 ATOM 527 O ASP A 776 −31.354 14.609 −7.411 1.00 43.09 ATOM 528 CB ASP A 776 −31.442 13.853 −4.762 1.00 51.21 ATOM 529 CG ASP A 776 −31.736 12.519 −5.434 1.00 54.67 ATOM 530 OD1 ASP A 776 −30.795 11.880 −5.970 1.00 54.64 ATOM 531 OD2 ASP A 776 −32.919 12.105 −5.407 1.00 56.04 ATOM 532 N HIS A 777 −29.110 14.797 −7.428 1.00 45.15 ATOM 533 CA HIS A 777 −28.977 14.929 −8.862 1.00 43.19 ATOM 534 C HIS A 777 −27.687 14.220 −9.231 1.00 44.58 ATOM 535 O HIS A 777 −26.690 14.324 −8.524 1.00 43.08 ATOM 536 CB HIS A 777 −28.899 16.401 −9.239 1.00 41.16 ATOM 537 CG HIS A 777 −28.776 16.641 −10.705 1.00 42.58 ATOM 538 ND1 HIS A 777 −27.601 16.439 −11.397 1.00 42.84 ATOM 539 CD2 HIS A 777 −29.684 17.063 −11.616 1.00 40.33 ATOM 540 CE1 HIS A 777 −27.791 16.728 −12.672 1.00 42.28 ATOM 541 NE2 HIS A 777 −29.047 17.109 −12.830 1.00 41.77 ATOM 542 N PRO A 778 −27.690 13.484 −10.350 1.00 46.58 ATOM 543 CA PRO A 778 −26.485 12.763 −10.768 1.00 47.00 ATOM 544 C PRO A 778 −25.241 13.622 −10.969 1.00 47.70 ATOM 545 O PRO A 778 −24.113 13.150 −10.775 1.00 48.99 ATOM 546 CB PRO A 778 −26.930 12.047 −12.046 1.00 45.89 ATOM 547 CG PRO A 778 −28.008 12.925 −12.575 1.00 45.82 ATOM 548 CD PRO A 778 −28.773 13.323 −11.338 1.00 45.42 ATOM 549 N HIS A 779 −25.415 14.890 −11.318 1.00 46.96 ATOM 550 CA HIS A 779 −24.231 15.701 −11.533 1.00 46.65 ATOM 551 C HIS A 779 −23.869 16.697 −10.426 1.00 46.00 ATOM 552 O HIS A 779 −23.195 17.709 −10.640 1.00 43.82 ATOM 553 CB HIS A 779 −24.318 16.330 −12.922 1.00 45.35 ATOM 554 CG HIS A 779 −24.475 15.309 −14.009 1.00 46.09 ATOM 555 ND1 HIS A 779 −23.614 14.242 −14.153 1.00 45.56 ATOM 556 CD2 HIS A 779 −25.423 15.156 −14.966 1.00 46.11 ATOM 557 CE1 HIS A 779 −24.025 13.476 −15.148 1.00 44.45 ATOM 558 NE2 HIS A 779 −25.121 14.008 −15.658 1.00 43.34 ATOM 559 N LEU A 780 −24.307 16.364 −9.222 1.00 45.67 ATOM 560 CA LEU A 780 −23.985 17.141 −8.038 1.00 48.21 ATOM 561 C LEU A 780 −23.651 16.086 −6.994 1.00 48.90 ATOM 562 O LEU A 780 −24.192 14.979 −7.029 1.00 48.98 ATOM 563 CB LEU A 780 −25.176 17.986 −7.572 1.00 48.42 ATOM 564 CG LEU A 780 −25.561 19.240 −8.367 1.00 49.03 ATOM 565 CD1 LEU A 780 −26.749 19.886 −7.683 1.00 49.91 ATOM 566 CD2 LEU A 780 −24.408 20.229 −8.432 1.00 47.36 ATOM 567 N VAL A 781 −22.746 16.398 −6.081 1.00 49.42 ATOM 568 CA VAL A 781 −22.413 15.420 −5.060 1.00 51.41 ATOM 569 C VAL A 781 −23.365 15.572 −3.882 1.00 53.85 ATOM 570 O VAL A 781 −24.077 16.572 −3.762 1.00 53.60 ATOM 571 CB VAL A 781 −20.969 15.592 −4.564 1.00 49.34 ATOM 572 CG1 VAL A 781 −19.998 15.434 −5.730 1.00 48.15 ATOM 573 CG2 VAL A 781 −20.809 16.942 −3.910 1.00 48.13 ATOM 574 N ARG A 782 −23.386 14.565 −3.018 1.00 57.31 ATOM 575 CA ARG A 782 −24.238 14.593 −1.834 1.00 58.51 ATOM 576 C ARG A 782 −23.429 14.365 −0.560 1.00 57.98 ATOM 577 O ARG A 782 −22.467 13.589 −0.537 1.00 58.11 ATOM 578 CB ARG A 782 −25.343 13.539 −1.943 1.00 59.06 ATOM 579 CG ARG A 782 −26.213 13.466 −0.718 1.00 64.02 ATOM 580 CD ARG A 782 −27.508 12.723 −0.986 1.00 69.63 ATOM 581 NE ARG A 782 −28.200 12.383 0.259 1.00 74.15 ATOM 582 CZ ARG A 782 −29.459 11.955 0.325 1.00 77.34 ATOM 583 NH1 ARG A 782 −30.173 11.821 −0.793 1.00 76.96 ATOM 584 NH2 ARG A 782 −29.999 11.642 1.504 1.00 76.96 ATOM 585 N LEU A 783 −23.817 15.063 0.497 1.00 57.15 ATOM 586 CA LEU A 783 −23.146 14.930 1.776 1.00 57.64 ATOM 587 C LEU A 783 −23.644 13.666 2.470 1.00 57.90 ATOM 588 O LEU A 783 −24.824 13.568 2.811 1.00 58.39 ATOM 589 CB LEU A 783 −23.454 16.147 2.649 1.00 56.99 ATOM 590 CG LEU A 783 −22.693 16.228 3.970 1.00 55.50 ATOM 591 CD1 LEU A 783 −21.204 16.354 3.679 1.00 54.23 ATOM 592 CD2 LEU A 783 −23.189 17.409 4.771 1.00 53.18 ATOM 593 N LEU A 784 −22.755 12.698 2.671 1.00 57.71 ATOM 594 CA LEU A 784 −23.137 11.456 3.341 1.00 57.94 ATOM 595 C LEU A 784 −23.412 11.744 4.809 1.00 57.07 ATOM 596 O LEU A 784 −24.453 11.360 5.353 1.00 57.68 ATOM 597 CB LEU A 784 −22.020 10.416 3.249 1.00 58.52 ATOM 598 CG LEU A 784 −21.758 9.742 1.905 1.00 61.56 ATOM 599 CD1 LEU A 784 −20.493 8.905 2.013 1.00 62.06 ATOM 600 CD2 LEU A 784 −22.950 8.881 1.499 1.00 60.90 ATOM 601 N GLY A 785 −22.472 12.433 5.446 1.00 55.42 ATOM 602 CA GLY A 785 −22.635 12.742 6.848 1.00 54.66 ATOM 603 C GLY A 785 −21.732 13.831 7.380 1.00 54.77 ATOM 604 O GLY A 785 −20.882 14.378 6.677 1.00 53.15 ATOM 605 N VAL A 786 −21.933 14.152 8.649 1.00 55.12 ATOM 606 CA VAL A 786 −21.147 15.177 9.300 1.00 55.18 ATOM 607 C VAL A 786 −20.685 14.649 10.638 1.00 56.04 ATOM 608 O VAL A 786 −21.445 13.976 11.337 1.00 57.35 ATOM 609 CB VAL A 786 −21.983 16.449 9.546 1.00 55.04 ATOM 610 CG1 VAL A 786 −21.148 17.477 10.282 1.00 54.87 ATOM 611 CG2 VAL A 786 −22.471 17.024 8.226 1.00 54.17 ATOM 612 N CYS A 787 −19.432 14.927 10.982 1.00 56.35 ATOM 613 CA CYS A 787 −18.900 14.517 12.274 1.00 56.07 ATOM 614 C CYS A 787 −18.624 15.800 13.043 1.00 55.27 ATOM 615 O CYS A 787 −17.881 16.661 12.579 1.00 53.31 ATOM 616 CB CYS A 787 −17.608 13.718 12.128 1.00 57.61 ATOM 617 SG CYS A 787 −16.830 13.406 13.747 1.00 65.10 ATOM 618 N LEU A 788 −19.216 15.918 14.222 1.00 56.11 ATOM 619 CA LEU A 788 −19.062 17.115 15.032 1.00 59.11 ATOM 620 C LEU A 788 −17.748 17.221 15.816 1.00 62.37 ATOM 621 O LEU A 788 −17.417 18.290 16.337 1.00 62.61 ATOM 622 CB LEU A 788 −20.250 17.220 15.987 1.00 56.56 ATOM 623 CG LEU A 788 −21.630 17.156 15.312 1.00 56.06 ATOM 624 CD1 LEU A 788 −22.708 17.085 16.375 1.00 53.74 ATOM 625 CD2 LEU A 788 −21.851 18.363 14.409 1.00 53.03 ATOM 626 N SER A 789 −16.991 16.130 15.893 1.00 65.37 ATOM 627 CA SER A 789 −15.732 16.142 16.641 1.00 68.05 ATOM 628 C SER A 789 −14.485 15.926 15.791 1.00 68.52 ATOM 629 O SER A 789 −14.522 15.191 14.805 1.00 69.20 ATOM 630 CB SER A 789 −15.767 15.078 17.739 1.00 68.67 ATOM 631 OG SER A 789 −14.457 14.804 18.207 1.00 72.14 ATOM 632 N PRO A 790 −13.365 16.587 16.154 1.00 69.26 ATOM 633 CA PRO A 790 −13.256 17.506 17.299 1.00 69.34 ATOM 634 C PRO A 790 −13.945 18.796 16.889 1.00 69.49 ATOM 635 O PRO A 790 −14.528 19.515 17.702 1.00 69.32 ATOM 636 CB PRO A 790 −11.750 17.677 17.458 1.00 68.09 ATOM 637 CG PRO A 790 −11.257 17.571 16.042 1.00 68.60 ATOM 638 CD PRO A 790 −12.051 16.403 15.507 1.00 68.85 ATOM 639 N THR A 791 −13.844 19.065 15.595 1.00 69.16 ATOM 640 CA THR A 791 −14.461 20.211 14.964 1.00 69.04 ATOM 641 C THR A 791 −15.183 19.583 13.787 1.00 67.87 ATOM 642 O THR A 791 −14.762 18.547 13.266 1.00 67.60 ATOM 643 CB THR A 791 −13.425 21.225 14.447 1.00 70.57 ATOM 644 OG1 THR A 791 −12.586 20.599 13.466 1.00 70.47 ATOM 645 CG2 THR A 791 −12.577 21.743 15.601 1.00 72.25 ATOM 646 N ILE A 792 −16.275 20.208 13.380 1.00 65.93 ATOM 647 CA ILE A 792 −17.081 19.707 12.288 1.00 63.52 ATOM 648 C ILE A 792 −16.307 19.199 11.082 1.00 61.83 ATOM 649 O ILE A 792 −15.436 19.882 10.551 1.00 60.85 ATOM 650 CB ILE A 792 −18.091 20.771 11.853 1.00 63.29 ATOM 651 CG1 ILE A 792 −19.080 21.014 13.001 1.00 63.31 ATOM 652 CG2 ILE A 792 −18.790 20.323 10.607 1.00 63.07 ATOM 653 CD1 ILE A 792 −20.228 21.943 12.680 1.00 66.80 ATOM 654 N GLN A 793 −16.642 17.983 10.666 1.00 61.24 ATOM 655 CA GLN A 793 −15.999 17.350 9.526 1.00 61.88 ATOM 656 C GLN A 793 −17.060 16.918 8.522 1.00 60.80 ATOM 657 O GLN A 793 −18.049 16.272 8.885 1.00 59.39 ATOM 658 CB GLN A 793 −15.196 16.122 9.968 1.00 63.66 ATOM 659 CG GLN A 793 −14.283 16.345 11.166 1.00 64.96 ATOM 660 CD GLN A 793 −13.435 15.123 11.493 1.00 66.60 ATOM 661 OE1 GLN A 793 −13.341 14.190 10.695 1.00 68.16 ATOM 662 NE2 GLN A 793 −12.824 15.119 12.676 1.00 67.52 ATOM 663 N LEU A 794 −16.841 17.282 7.260 1.00 59.86 ATOM 664 CA LEU A 794 −17.759 16.946 6.181 1.00 58.57 ATOM 665 C LEU A 794 −17.334 15.628 5.571 1.00 58.29 ATOM 666 O LEU A 794 −16.141 15.357 5.441 1.00 58.99 ATOM 667 CB LEU A 794 −17.747 18.051 5.128 1.00 59.01 ATOM 668 CG LEU A 794 −18.194 19.414 5.668 1.00 58.65 ATOM 669 CD1 LEU A 794 −18.223 20.438 4.546 1.00 58.33 ATOM 670 CD2 LEU A 794 −19.573 19.276 6.298 1.00 57.68 ATOM 671 N VAL A 795 −18.311 14.807 5.199 1.00 58.23 ATOM 672 CA VAL A 795 −18.025 13.493 4.635 1.00 57.20 ATOM 673 C VAL A 795 −18.868 13.178 3.411 1.00 58.75 ATOM 674 O VAL A 795 −20.096 13.062 3.490 1.00 57.69 ATOM 675 CB VAL A 795 −18.257 12.371 5.680 1.00 55.92 ATOM 676 CG1 VAL A 795 −17.708 11.054 5.163 1.00 55.27 ATOM 677 CG2 VAL A 795 −17.604 12.740 7.003 1.00 54.71 ATOM 678 N THR A 796 −18.184 13.025 2.283 1.00 60.18 ATOM 679 CA THR A 796 −18.824 12.716 1.018 1.00 63.32 ATOM 680 C THR A 796 −18.246 11.432 0.461 1.00 64.55 ATOM 681 O THR A 796 −17.150 11.012 0.838 1.00 64.79 ATOM 682 CB THR A 796 −18.555 13.799 −0.050 1.00 63.87 ATOM 683 OG1 THR A 796 −18.802 15.099 0.494 1.00 67.06 ATOM 684 CG2 THR A 796 −19.463 13.586 −1.255 1.00 63.95 ATOM 685 N GLN A 797 −18.991 10.815 −0.445 1.00 65.24 ATOM 686 CA GLN A 797 −18.522 9.611 −1.100 1.00 66.49 ATOM 687 C GLN A 797 −17.288 10.093 −1.848 1.00 66.60 ATOM 688 O GLN A 797 −17.234 11.249 −2.278 1.00 67.28 ATOM 689 CB GLN A 797 −19.569 9.120 −2.089 1.00 67.59 ATOM 690 CG GLN A 797 −19.197 7.860 −2.834 1.00 71.35 ATOM 691 CD GLN A 797 −20.192 7.552 −3.940 1.00 74.61 ATOM 692 OE1 GLN A 797 −21.400 7.453 −3.696 1.00 75.46 ATOM 693 NE2 GLN A 797 −19.693 7.405 −5.166 1.00 74.15 ATOM 694 N LEU A 798 −16.287 9.234 −1.986 1.00 65.62 ATOM 695 CA LEU A 798 −15.082 9.631 −2.697 1.00 64.21 ATOM 696 C LEU A 798 −15.309 9.410 −4.187 1.00 65.69 ATOM 697 O LEU A 798 −16.029 8.487 −4.582 1.00 66.02 ATOM 698 CB LEU A 798 −13.888 8.801 −2.228 1.00 61.04 ATOM 699 CG LEU A 798 −12.541 9.140 −2.860 1.00 60.59 ATOM 700 CD1 LEU A 798 −12.125 10.543 −2.451 1.00 60.17 ATOM 701 CD2 LEU A 798 −11.498 8.133 −2.415 1.00 59.95 ATOM 702 N MET A 799 −14.722 10.272 −5.013 1.00 65.98 ATOM 703 CA MET A 799 −14.846 10.135 −6.459 1.00 65.14 ATOM 704 C MET A 799 −13.531 9.518 −6.915 1.00 64.98 ATOM 705 O MET A 799 −12.497 10.186 −6.964 1.00 65.11 ATOM 706 CB MET A 799 −15.076 11.499 −7.123 1.00 64.55 ATOM 707 CG MET A 799 −16.418 12.140 −6.791 1.00 62.41 ATOM 708 SD MET A 799 −17.821 11.182 −7.391 1.00 63.79 ATOM 709 CE MET A 799 −18.278 10.242 −5.953 1.00 63.53 ATOM 710 N PRO A 800 −13.559 8.221 −7.249 1.00 65.17 ATOM 711 CA PRO A 800 −12.386 7.464 −7.697 1.00 65.94 ATOM 712 C PRO A 800 −11.452 8.149 −8.692 1.00 65.86 ATOM 713 O PRO A 800 −10.254 8.255 −8.443 1.00 64.64 ATOM 714 CB PRO A 800 −12.999 6.173 −8.257 1.00 66.48 ATOM 715 CG PRO A 800 −14.391 6.583 −8.651 1.00 65.65 ATOM 716 CD PRO A 800 −14.792 7.454 −7.496 1.00 65.28 ATOM 717 N HIS A 801 −11.998 8.614 −9.811 1.00 66.24 ATOM 718 CA HIS A 801 −11.185 9.251 −10.834 1.00 66.32 ATOM 719 C HIS A 801 −10.814 10.712 −10.584 1.00 65.51 ATOM 720 O HIS A 801 −10.474 11.439 −11.512 1.00 66.97 ATOM 721 CB HIS A 801 −11.861 9.082 −12.195 1.00 68.47 ATOM 722 CG HIS A 801 −11.882 7.661 −12.679 1.00 70.66 ATOM 723 ND1 HIS A 801 −10.742 6.990 −13.071 1.00 70.46 ATOM 724 CD2 HIS A 801 −12.900 6.773 −12.798 1.00 71.35 ATOM 725 CE1 HIS A 801 −11.057 5.751 −13.407 1.00 70.98 ATOM 726 NE2 HIS A 801 −12.359 5.593 −13.250 1.00 71.18 ATOM 727 N GLY A 802 −10.885 11.130 −9.324 1.00 64.19 ATOM 728 CA GLY A 802 −10.503 12.479 −8.929 1.00 61.92 ATOM 729 C GLY A 802 −11.137 13.756 −9.473 1.00 60.42 ATOM 730 O GLY A 802 −12.277 13.794 −9.935 1.00 57.28 ATOM 731 N CYS A 803 −10.355 14.825 −9.374 1.00 59.58 ATOM 732 CA CYS A 803 −10.755 16.146 −9.812 1.00 58.64 ATOM 733 C CYS A 803 −10.613 16.269 −11.316 1.00 59.22 ATOM 734 O CYS A 803 −9.576 15.912 −11.881 1.00 59.33 ATOM 735 CB CYS A 803 −9.891 17.202 −9.123 1.00 58.78 ATOM 736 SG CYS A 803 −10.148 17.335 −7.322 1.00 60.97 ATOM 737 N LEU A 804 −11.660 16.786 −11.955 1.00 58.47 ATOM 738 CA LEU A 804 −11.686 16.960 −13.399 1.00 57.67 ATOM 739 C LEU A 804 −10.524 17.792 −13.938 1.00 57.23 ATOM 740 O LEU A 804 −9.973 17.494 −14.995 1.00 57.42 ATOM 741 CB LEU A 804 −13.010 17.592 −13.822 1.00 57.36 ATOM 742 CG LEU A 804 −13.136 17.853 −15.323 1.00 56.02 ATOM 743 CD1 LEU A 804 −12.864 16.566 −16.073 1.00 56.06 ATOM 744 CD2 LEU A 804 −14.522 18.392 −15.646 1.00 56.14 ATOM 745 N LEU A 805 −10.151 18.839 −13.219 1.00 56.60 ATOM 746 CA LEU A 805 −9.054 19.674 −13.666 1.00 57.25 ATOM 747 C LEU A 805 −7.770 18.871 −13.836 1.00 59.50 ATOM 748 O LEU A 805 −7.068 19.041 −14.826 1.00 61.05 ATOM 749 CB LEU A 805 −8.821 20.814 −12.681 1.00 54.99 ATOM 750 CG LEU A 805 −7.600 21.668 −12.995 1.00 52.96 ATOM 751 CD1 LEU A 805 −7.614 22.102 −14.453 1.00 51.15 ATOM 752 CD2 LEU A 805 −7.596 22.863 −12.072 1.00 53.82 ATOM 753 N GLU A 806 −7.458 18.006 −12.873 1.00 61.71 ATOM 754 CA GLU A 806 −6.249 17.186 −12.952 1.00 64.25 ATOM 755 C GLU A 806 −6.435 16.119 −14.027 1.00 63.97 ATOM 756 O GLU A 806 −5.477 15.676 −14.665 1.00 63.45 ATOM 757 CB GLU A 806 −5.957 16.495 −11.611 1.00 67.06 ATOM 758 CG GLU A 806 −5.509 17.425 −10.477 1.00 73.60 ATOM 759 CD GLU A 806 −5.169 16.666 −9.188 1.00 76.72 ATOM 760 OE1 GLU A 806 −5.484 15.455 −9.105 1.00 77.37 ATOM 761 OE2 GLU A 806 −4.593 17.279 −8.259 1.00 78.10 ATOM 762 N TYR A 807 −7.684 15.719 −14.228 1.00 63.27 ATOM 763 CA TYR A 807 −8.015 14.694 −15.203 1.00 63.32 ATOM 764 C TYR A 807 −7.749 15.098 −16.649 1.00 62.69 ATOM 765 O TYR A 807 −7.050 14.391 −17.364 1.00 61.57 ATOM 766 CB TYR A 807 −9.478 14.294 −15.058 1.00 63.62 ATOM 767 CG TYR A 807 −9.822 13.015 −15.769 1.00 63.28 ATOM 768 CD1 TYR A 807 −9.545 11.778 −15.189 1.00 62.76 ATOM 769 CD2 TYR A 807 −10.436 13.040 −17.017 1.00 63.66 ATOM 770 CE1 TYR A 807 −9.879 10.597 −15.834 1.00 63.41 ATOM 771 CE2 TYR A 807 −10.771 11.867 −17.671 1.00 64.64 ATOM 772 CZ TYR A 807 −10.494 10.650 −17.074 1.00 64.30 ATOM 773 OH TYR A 807 −10.854 9.494 −17.719 1.00 65.98 ATOM 774 N VAL A 808 −8.305 16.223 −17.087 1.00 62.57 ATOM 775 CA VAL A 808 −8.087 16.644 −18.466 1.00 64.21 ATOM 776 C VAL A 808 −6.626 16.901 −18.773 1.00 65.63 ATOM 777 O VAL A 808 −6.238 16.927 −19.933 1.00 66.29 ATOM 778 CB VAL A 808 −8.865 17.914 −18.831 1.00 61.95 ATOM 779 CG1 VAL A 808 −10.337 17.614 −18.891 1.00 61.31 ATOM 780 CG2 VAL A 808 −8.568 19.003 −17.832 1.00 61.93 ATOM 781 N HIS A 809 −5.811 17.093 −17.746 1.00 68.17 ATOM 782 CA HIS A 809 −4.398 17.337 −17.986 1.00 72.57 ATOM 783 C HIS A 809 −3.690 16.011 −18.246 1.00 72.86 ATOM 784 O HIS A 809 −3.024 15.834 −19.266 1.00 73.15 ATOM 785 CB HIS A 809 −3.756 18.034 −16.787 1.00 76.24 ATOM 786 CG HIS A 809 −2.334 18.446 −17.018 1.00 80.69 ATOM 787 ND1 HIS A 809 −1.989 19.505 −17.831 1.00 82.82 ATOM 788 CD2 HIS A 809 −1.169 17.940 −16.544 1.00 82.57 ATOM 789 CE1 HIS A 809 −0.673 19.635 −17.846 1.00 83.54 ATOM 790 NE2 HIS A 809 −0.152 18.698 −17.074 1.00 83.63 ATOM 791 N GLU A 810 −3.851 15.077 −17.320 1.00 73.25 ATOM 792 CA GLU A 810 −3.220 13.776 −17.441 1.00 74.27 ATOM 793 C GLU A 810 −3.700 12.994 −18.655 1.00 73.56 ATOM 794 O GLU A 810 −2.901 12.341 −19.331 1.00 73.89 ATOM 795 CB GLU A 810 −3.466 12.963 −16.172 1.00 76.41 ATOM 796 CG GLU A 810 −2.767 13.517 −14.941 1.00 80.78 ATOM 797 CD GLU A 810 −3.185 12.795 −13.670 1.00 84.23 ATOM 798 OE1 GLU A 810 −3.195 11.542 −13.672 1.00 85.68 ATOM 799 OE2 GLU A 810 −3.498 13.479 −12.668 1.00 84.74 ATOM 800 N HIS A 811 −4.998 13.070 −18.937 1.00 72.66 ATOM 801 CA HIS A 811 −5.582 12.346 −20.063 1.00 72.30 ATOM 802 C HIS A 811 −5.823 13.195 −21.303 1.00 72.06 ATOM 803 O HIS A 811 −6.591 12.801 −22.187 1.00 71.12 ATOM 804 CB HIS A 811 −6.899 11.701 −19.638 1.00 73.09 ATOM 805 CG HIS A 811 −6.750 10.700 −18.539 1.00 74.95 ATOM 806 ND1 HIS A 811 −6.018 10.951 −17.399 1.00 76.95 ATOM 807 CD2 HIS A 811 −7.260 9.455 −18.392 1.00 76.68 ATOM 808 CE1 HIS A 811 −6.084 9.904 −16.596 1.00 77.89 ATOM 809 NE2 HIS A 811 −6.833 8.983 −17.175 1.00 77.93 ATOM 810 N LYS A 812 −5.167 14.351 −21.369 1.00 72.19 ATOM 811 CA LYS A 812 −5.321 15.247 −22.510 1.00 72.68 ATOM 812 C LYS A 812 −5.330 14.462 −23.805 1.00 73.33 ATOM 813 O LYS A 812 −6.280 14.518 −24.584 1.00 73.60 ATOM 814 CB LYS A 812 −4.180 16.271 −22.570 1.00 72.21 ATOM 815 CG LYS A 812 −4.116 16.982 −23.917 1.00 71.18 ATOM 816 CD LYS A 812 −3.146 18.148 −23.951 1.00 70.28 ATOM 817 CE LYS A 812 −3.235 18.834 −25.308 1.00 68.88 ATOM 818 NZ LYS A 812 −2.481 20.108 −25.344 1.00 68.31 ATOM 819 N ASP A 813 −4.256 13.717 −24.015 1.00 75.12 ATOM 820 CA ASP A 813 −4.092 12.917 −25.213 1.00 76.11 ATOM 821 C ASP A 813 −5.038 11.712 −25.213 1.00 75.70 ATOM 822 O ASP A 813 −4.692 10.641 −25.697 1.00 75.57 ATOM 823 CB ASP A 813 −2.627 12.469 −25.312 1.00 78.16 ATOM 824 CG ASP A 813 −1.639 13.629 −25.104 1.00 79.48 ATOM 825 OD1 ASP A 813 −1.703 14.618 −25.867 1.00 78.24 ATOM 826 OD2 ASP A 813 −0.795 13.554 −24.176 1.00 81.15 ATOM 827 N ASN A 814 −6.237 11.901 −24.671 1.00 75.59 ATOM 828 CA ASN A 814 −7.232 10.835 −24.609 1.00 75.15 ATOM 829 C ASN A 814 −8.639 11.421 −24.602 1.00 73.09 ATOM 830 O ASN A 814 −9.629 10.690 −24.620 1.00 72.17 ATOM 831 CB ASN A 814 −7.038 10.003 −23.340 1.00 79.73 ATOM 832 CG ASN A 814 −8.095 8.910 −23.182 1.00 83.39 ATOM 833 OD1 ASN A 814 −8.417 8.495 −22.059 1.00 85.44 ATOM 834 ND2 ASN A 814 −8.628 8.429 −24.306 1.00 82.76 ATOM 835 N ILE A 815 −8.725 12.746 −24.575 1.00 70.07 ATOM 836 CA ILE A 815 −10.018 13.414 −24.543 1.00 66.45 ATOM 837 C ILE A 815 −10.548 13.773 −25.923 1.00 64.58 ATOM 838 O ILE A 815 −9.910 14.515 −26.670 1.00 65.16 ATOM 839 CB ILE A 815 −9.940 14.686 −23.701 1.00 66.17 ATOM 840 CG1 ILE A 815 −9.416 14.337 −22.310 1.00 64.41 ATOM 841 CG2 ILE A 815 −11.308 15.341 −23.616 1.00 65.95 ATOM 842 CD1 ILE A 815 −10.283 13.377 −21.576 1.00 64.44 ATOM 843 N GLY A 816 −11.727 13.244 −26.244 1.00 61.95 ATOM 844 CA GLY A 816 −12.348 13.502 −27.529 1.00 58.49 ATOM 845 C GLY A 816 −13.391 14.602 −27.474 1.00 57.57 ATOM 846 O GLY A 816 −13.798 15.049 −26.400 1.00 56.05 ATOM 847 N SER A 817 −13.836 15.036 −28.645 1.00 55.76 ATOM 848 CA SER A 817 −14.814 16.100 −28.723 1.00 54.42 ATOM 849 C SER A 817 −16.087 15.748 −27.976 1.00 53.51 ATOM 850 O SER A 817 −16.653 16.588 −27.277 1.00 53.70 ATOM 851 CB SER A 817 −15.140 16.417 −30.188 1.00 54.21 ATOM 852 OG SER A 817 −15.754 15.315 −30.830 1.00 53.76 ATOM 853 N GLN A 818 −16.526 14.503 −28.118 1.00 52.59 ATOM 854 CA GLN A 818 −17.755 14.046 −27.481 1.00 52.58 ATOM 855 C GLN A 818 −17.711 14.105 −25.962 1.00 52.52 ATOM 856 O GLN A 818 −18.606 14.649 −25.316 1.00 53.30 ATOM 857 CB GLN A 818 −18.071 12.624 −27.929 1.00 52.77 ATOM 858 CG GLN A 818 −19.386 12.096 −27.396 1.00 55.94 ATOM 859 CD GLN A 818 −19.734 10.728 −27.960 1.00 57.95 ATOM 860 OE1 GLN A 818 −19.015 9.749 −27.741 1.00 55.96 ATOM 861 NE2 GLN A 818 −20.841 10.657 −28.694 1.00 58.90 ATOM 862 N LEU A 819 −16.663 13.535 −25.392 1.00 52.33 ATOM 863 CA LEU A 819 −16.487 13.519 −23.951 1.00 53.05 ATOM 864 C LEU A 819 −16.530 14.955 −23.374 1.00 52.97 ATOM 865 O LEU A 819 −17.199 15.211 −22.372 1.00 51.99 ATOM 866 CB LEU A 819 −15.147 12.846 −23.641 1.00 55.20 ATOM 867 CG LEU A 819 −14.857 12.305 −22.246 1.00 58.07 ATOM 868 CD1 LEU A 819 −15.883 11.248 −21.893 1.00 59.70 ATOM 869 CD2 LEU A 819 −13.454 11.722 −22.216 1.00 57.59 ATOM 870 N LEU A 820 −15.823 15.881 −24.024 1.00 51.18 ATOM 871 CA LEU A 820 −15.761 17.274 −23.592 1.00 49.17 ATOM 872 C LEU A 820 −17.089 18.021 −23.663 1.00 48.89 ATOM 873 O LEU A 820 −17.395 18.820 −22.776 1.00 48.95 ATOM 874 CB LEU A 820 −14.725 18.041 −24.415 1.00 48.36 ATOM 875 CG LEU A 820 −13.252 17.791 −24.106 1.00 47.62 ATOM 876 CD1 LEU A 820 −12.411 18.277 −25.275 1.00 47.48 ATOM 877 CD2 LEU A 820 −12.859 18.485 −22.813 1.00 46.35 ATOM 878 N LEU A 821 −17.867 17.794 −24.719 1.00 47.18 ATOM 879 CA LEU A 821 −19.158 18.470 −24.845 1.00 45.74 ATOM 880 C LEU A 821 −20.174 17.912 −23.858 1.00 44.93 ATOM 881 O LEU A 821 −21.035 18.636 −23.366 1.00 44.43 ATOM 882 CB LEU A 821 −19.699 18.350 −26.269 1.00 43.56 ATOM 883 CG LEU A 821 −19.043 19.245 −27.324 1.00 44.32 ATOM 884 CD1 LEU A 821 −19.595 18.904 −28.686 1.00 42.72 ATOM 885 CD2 LEU A 821 −19.299 20.706 −27.015 1.00 41.61 ATOM 886 N ASN A 822 −20.074 16.620 −23.575 1.00 45.14 ATOM 887 CA ASN A 822 −20.978 15.992 −22.630 1.00 46.84 ATOM 888 C ASN A 822 −20.710 16.514 −21.216 1.00 46.44 ATOM 889 O ASN A 822 −21.629 16.712 −20.429 1.00 47.65 ATOM 890 CB ASN A 822 −20.803 14.480 −22.683 1.00 50.43 ATOM 891 CG ASN A 822 −21.407 13.874 −23.930 1.00 53.27 ATOM 892 OD1 ASN A 822 −22.624 13.914 −24.127 1.00 55.44 ATOM 893 ND2 ASN A 822 −20.564 13.310 −24.782 1.00 55.67 ATOM 894 N TRP A 823 −19.448 16.736 −20.886 1.00 44.44 ATOM 895 CA TRP A 823 −19.126 17.265 −19.571 1.00 44.31 ATOM 896 C TRP A 823 −19.734 18.662 −19.418 1.00 42.62 ATOM 897 O TRP A 823 −20.172 19.051 −18.331 1.00 41.36 ATOM 898 CB TRP A 823 −17.609 17.334 −19.376 1.00 44.91 ATOM 899 CG TRP A 823 −16.949 15.987 −19.186 1.00 46.37 ATOM 900 CD1 TRP A 823 −17.551 14.826 −18.785 1.00 45.40 ATOM 901 CD2 TRP A 823 −15.552 15.689 −19.318 1.00 46.95 ATOM 902 NE1 TRP A 823 −16.615 13.828 −18.656 1.00 46.44 ATOM 903 CE2 TRP A 823 −15.380 14.328 −18.977 1.00 46.59 ATOM 904 CE3 TRP A 823 −14.425 16.441 −19.693 1.00 49.03 ATOM 905 CZ2 TRP A 823 −14.128 13.699 −18.998 1.00 46.68 ATOM 906 CZ3 TRP A 823 −13.169 15.808 −19.715 1.00 50.33 ATOM 907 CH2 TRP A 823 −13.038 14.451 −19.368 1.00 47.90 ATOM 908 N CYS A 824 −19.773 19.407 −20.514 1.00 40.45 ATOM 909 CA CYS A 824 −20.329 20.746 −20.489 1.00 42.24 ATOM 910 C CYS A 824 −21.799 20.690 −20.146 1.00 43.66 ATOM 911 O CYS A 824 −22.309 21.548 −19.426 1.00 43.87 ATOM 912 CB CYS A 824 −20.138 21.439 −21.836 1.00 43.69 ATOM 913 SG CYS A 824 −18.428 21.910 −22.159 1.00 44.22 ATOM 914 N VAL A 825 −22.472 19.668 −20.667 1.00 45.00 ATOM 915 CA VAL A 825 −23.896 19.459 −20.425 1.00 42.03 ATOM 916 C VAL A 825 −24.109 19.061 −18.973 1.00 42.11 ATOM 917 O VAL A 825 −24.921 19.653 −18.254 1.00 40.65 ATOM 918 CB VAL A 825 −24.441 18.353 −21.337 1.00 41.91 ATOM 919 CG1 VAL A 825 −25.865 17.993 −20.940 1.00 41.30 ATOM 920 CG2 VAL A 825 −24.392 18.821 −22.788 1.00 41.84 ATOM 921 N GLN A 826 −23.362 18.053 −18.543 1.00 42.60 ATOM 922 CA GLN A 826 −23.460 17.573 −17.175 1.00 42.94 ATOM 923 C GLN A 826 −23.232 18.697 −16.182 1.00 40.98 ATOM 924 O GLN A 826 −24.012 18.858 −15.253 1.00 41.31 ATOM 925 CB GLN A 826 −22.475 16.428 −16.965 1.00 43.82 ATOM 926 CG GLN A 826 −22.954 15.187 −17.689 1.00 46.63 ATOM 927 CD GLN A 826 −21.996 14.029 −17.594 1.00 47.66 ATOM 928 OE1 GLN A 826 −21.205 13.938 −16.660 1.00 47.25 ATOM 929 NE2 GLN A 826 −22.077 13.119 −18.559 1.00 49.33 ATOM 930 N ILE A 827 −22.180 19.485 −16.381 1.00 39.59 ATOM 931 CA ILE A 827 −21.920 20.598 −15.479 1.00 38.36 ATOM 932 C ILE A 827 −23.090 21.596 −15.527 1.00 39.97 ATOM 933 O ILE A 827 −23.643 21.967 −14.485 1.00 41.14 ATOM 934 CB ILE A 827 −20.607 21.329 −15.834 1.00 36.75 ATOM 935 CG1 ILE A 827 −19.449 20.320 −15.852 1.00 36.42 ATOM 936 CG2 ILE A 827 −20.335 22.436 −14.816 1.00 32.91 ATOM 937 CD1 ILE A 827 −18.064 20.930 −15.996 1.00 33.58 ATOM 938 N ALA A 828 −23.479 22.016 −16.727 1.00 38.03 ATOM 939 CA ALA A 828 −24.581 22.957 −16.867 1.00 38.98 ATOM 940 C ALA A 828 −25.848 22.407 −16.203 1.00 41.61 ATOM 941 O ALA A 828 −26.562 23.133 −15.514 1.00 41.11 ATOM 942 CB ALA A 828 −24.835 23.253 −18.339 1.00 37.80 ATOM 943 N LYS A 829 −26.120 21.118 −16.398 1.00 43.40 ATOM 944 CA LYS A 829 −27.302 20.502 −15.803 1.00 43.58 ATOM 945 C LYS A 829 −27.298 20.557 −14.277 1.00 45.12 ATOM 946 O LYS A 829 −28.319 20.849 −13.666 1.00 45.69 ATOM 947 CB LYS A 829 −27.444 19.055 −16.272 1.00 43.15 ATOM 948 CG LYS A 829 −28.315 18.892 −17.508 1.00 43.32 ATOM 949 CD LYS A 829 −28.403 17.433 −17.912 1.00 47.16 ATOM 950 CE LYS A 829 −29.243 17.228 −19.164 1.00 49.43 ATOM 951 NZ LYS A 829 −29.209 15.792 −19.577 1.00 50.93 ATOM 952 N GLY A 830 −26.159 20.268 −13.661 1.00 46.16 ATOM 953 CA GLY A 830 −26.090 20.327 −12.214 1.00 46.02 ATOM 954 C GLY A 830 −26.349 21.744 −11.721 1.00 46.34 ATOM 955 O GLY A 830 −27.060 21.948 −10.729 1.00 46.09 ATOM 956 N MET A 831 −25.770 22.731 −12.399 1.00 45.04 ATOM 957 CA MET A 831 −25.982 24.119 −11.999 1.00 46.30 ATOM 958 C MET A 831 −27.484 24.407 −12.125 1.00 47.00 ATOM 959 O MET A 831 −28.076 25.117 −11.306 1.00 45.79 ATOM 960 CB MET A 831 −25.173 25.069 −12.896 1.00 43.99 ATOM 961 CG MET A 831 −23.675 24.923 −12.748 1.00 40.18 ATOM 962 SD MET A 831 −23.169 25.141 −11.023 1.00 41.93 ATOM 963 CE MET A 831 −23.711 26.840 −10.757 1.00 41.68 ATOM 964 N MET A 832 −28.084 23.819 −13.156 1.00 46.35 ATOM 965 CA MET A 832 −29.503 23.954 −13.444 1.00 48.31 ATOM 966 C MET A 832 −30.330 23.517 −12.236 1.00 47.54 ATOM 967 O MET A 832 −31.274 24.197 −11.828 1.00 49.03 ATOM 968 CB MET A 832 −29.835 23.080 −14.648 1.00 52.33 ATOM 969 CG MET A 832 −31.143 23.377 −15.345 1.00 57.13 ATOM 970 SD MET A 832 −31.249 22.334 −16.823 1.00 62.53 ATOM 971 CE MET A 832 −30.102 23.157 −17.832 1.00 58.95 ATOM 972 N TYR A 833 −29.963 22.375 −11.670 1.00 45.22 ATOM 973 CA TYR A 833 −30.637 21.832 −10.508 1.00 43.85 ATOM 974 C TYR A 833 −30.446 22.781 −9.332 1.00 45.57 ATOM 975 O TYR A 833 −31.382 23.033 −8.571 1.00 44.47 ATOM 976 CB TYR A 833 −30.041 20.475 −10.161 1.00 42.10 ATOM 977 CG TYR A 833 −30.709 19.759 −9.006 1.00 42.47 ATOM 978 CD1 TYR A 833 −31.781 18.877 −9.223 1.00 41.47 ATOM 979 CD2 TYR A 833 −30.226 19.902 −7.702 1.00 39.44 ATOM 980 CE1 TYR A 833 −32.344 18.143 −8.165 1.00 37.67 ATOM 981 CE2 TYR A 833 −30.784 19.184 −6.639 1.00 39.15 ATOM 982 CZ TYR A 833 −31.837 18.306 −6.877 1.00 38.87 ATOM 983 OH TYR A 833 −32.378 17.600 −5.827 1.00 38.16 ATOM 984 N LEU A 834 −29.232 23.304 −9.176 1.00 45.55 ATOM 985 CA LEU A 834 −28.958 24.225 −8.072 1.00 46.56 ATOM 986 C LEU A 834 −29.800 25.496 −8.168 1.00 45.77 ATOM 987 O LEU A 834 −30.432 25.894 −7.199 1.00 45.06 ATOM 988 CB LEU A 834 −27.468 24.601 −8.022 1.00 46.73 ATOM 989 CG LEU A 834 −26.445 23.528 −7.609 1.00 47.94 ATOM 990 CD1 LEU A 834 −25.044 24.081 −7.736 1.00 45.98 ATOM 991 CD2 LEU A 834 −26.679 23.094 −6.184 1.00 46.82 ATOM 992 N GLU A 835 −29.803 26.126 −9.337 1.00 46.46 ATOM 993 CA GLU A 835 −30.561 27.359 −9.559 1.00 48.02 ATOM 994 C GLU A 835 −32.059 27.172 −9.298 1.00 48.70 ATOM 995 O GLU A 835 −32.749 28.101 −8.872 1.00 44.97 ATOM 996 CB GLU A 835 −30.357 27.835 −10.997 1.00 48.88 ATOM 997 CG GLU A 835 −30.994 29.167 −11.320 1.00 51.38 ATOM 998 CD GLU A 835 −30.899 29.497 −12.791 1.00 55.29 ATOM 999 OE1 GLU A 835 −31.031 30.682 −13.160 1.00 61.79 ATOM 1000 OE2 GLU A 835 −30.699 28.562 −13.591 1.00 59.22 ATOM 1001 N GLU A 836 −32.547 25.966 −9.585 1.00 49.61 ATOM 1002 CA GLU A 836 −33.941 25.609 −9.393 1.00 51.33 ATOM 1003 C GLU A 836 −34.251 25.644 −7.893 1.00 52.42 ATOM 1004 O GLU A 836 −35.376 25.933 −7.476 1.00 53.59 ATOM 1005 CB GLU A 836 −34.172 24.213 −9.976 1.00 53.43 ATOM 1006 CG GLU A 836 −35.554 23.632 −9.752 1.00 61.91 ATOM 1007 CD GLU A 836 −35.694 22.222 −10.322 1.00 68.30 ATOM 1008 OE1 GLU A 836 −34.777 21.393 −10.103 1.00 70.37 ATOM 1009 OE2 GLU A 836 −36.723 21.938 −10.984 1.00 72.73 ATOM 1010 N ARG A 837 −33.232 25.366 −7.089 1.00 52.07 ATOM 1011 CA ARG A 837 −33.342 25.363 −5.632 1.00 53.28 ATOM 1012 C ARG A 837 −32.980 26.731 −5.018 1.00 53.42 ATOM 1013 O ARG A 837 −32.909 26.859 −3.800 1.00 52.59 ATOM 1014 CB ARG A 837 −32.401 24.300 −5.041 1.00 54.24 ATOM 1015 CG ARG A 837 −32.654 22.870 −5.507 1.00 54.61 ATOM 1016 CD ARG A 837 −33.996 22.419 −5.013 1.00 54.07 ATOM 1017 NE ARG A 837 −34.338 21.032 −5.316 1.00 54.63 ATOM 1018 CZ ARG A 837 −34.342 20.493 −6.529 1.00 53.35 ATOM 1019 NH1 ARG A 837 −33.993 21.207 −7.590 1.00 54.44 ATOM 1020 NH2 ARG A 837 −34.777 19.250 −6.687 1.00 52.90 ATOM 1021 N ARG A 838 −32.739 27.734 −5.862 1.00 54.60 ATOM 1022 CA ARG A 838 −32.366 29.084 −5.417 1.00 56.39 ATOM 1023 C ARG A 838 −30.963 29.097 −4.789 1.00 55.44 ATOM 1024 O ARG A 838 −30.669 29.912 −3.911 1.00 55.30 ATOM 1025 CB ARG A 838 −33.378 29.619 −4.393 1.00 60.89 ATOM 1026 CG ARG A 838 −34.852 29.577 −4.822 1.00 68.36 ATOM 1027 CD ARG A 838 −35.206 30.654 −5.846 1.00 73.13 ATOM 1028 NE ARG A 838 −36.650 30.723 −6.105 1.00 77.28 ATOM 1029 CZ ARG A 838 −37.320 29.908 −6.920 1.00 78.68 ATOM 1030 NH1 ARG A 838 −38.629 30.061 −7.074 1.00 78.70 ATOM 1031 NH2 ARG A 838 −36.686 28.951 −7.592 1.00 78.88 ATOM 1032 N LEU A 839 −30.091 28.207 −5.253 1.00 52.78 ATOM 1033 CA LEU A 839 −28.744 28.115 −4.703 1.00 50.80 ATOM 1034 C LEU A 839 −27.635 28.587 −5.644 1.00 49.61 ATOM 1035 O LEU A 839 −27.558 28.180 −6.801 1.00 51.46 ATOM 1036 CB LEU A 839 −28.472 26.674 −4.275 1.00 51.33 ATOM 1037 CG LEU A 839 −29.535 26.036 −3.370 1.00 52.40 ATOM 1038 CD1 LEU A 839 −29.216 24.548 −3.176 1.00 51.01 ATOM 1039 CD2 LEU A 839 −29.593 26.778 −2.026 1.00 50.05 ATOM 1040 N VAL A 840 −26.773 29.455 −5.138 1.00 46.94 ATOM 1041 CA VAL A 840 −25.671 29.958 −5.933 1.00 45.16 ATOM 1042 C VAL A 840 −24.388 29.267 −5.497 1.00 45.42 ATOM 1043 O VAL A 840 −24.124 29.147 −4.309 1.00 45.89 ATOM 1044 CB VAL A 840 −25.515 31.472 −5.750 1.00 44.00 ATOM 1045 CG1 VAL A 840 −24.412 32.005 −6.673 1.00 39.24 ATOM 1046 CG2 VAL A 840 −26.846 32.150 −6.036 1.00 42.54 ATOM 1047 N HIS A 841 −23.588 28.805 −6.450 1.00 45.68 ATOM 1048 CA HIS A 841 −22.343 28.137 −6.097 1.00 45.32 ATOM 1049 C HIS A 841 −21.307 29.133 −5.578 1.00 45.51 ATOM 1050 O HIS A 841 −20.752 28.958 −4.496 1.00 46.26 ATOM 1051 CB HIS A 841 −21.778 27.396 −7.305 1.00 44.31 ATOM 1052 CG HIS A 841 −20.707 26.410 −6.956 1.00 43.65 ATOM 1053 ND1 HIS A 841 −19.583 26.755 −6.240 1.00 41.64 ATOM 1054 CD2 HIS A 841 −20.592 25.088 −7.222 1.00 43.78 ATOM 1055 CE1 HIS A 841 −18.821 25.689 −6.080 1.00 42.85 ATOM 1056 NE2 HIS A 841 −19.410 24.664 −6.667 1.00 43.25 ATOM 1057 N ARG A 842 −21.050 30.173 −6.363 1.00 46.38 ATOM 1058 CA ARG A 842 −20.086 31.213 −6.009 1.00 48.44 ATOM 1059 C ARG A 842 −18.643 30.854 −6.304 1.00 47.29 ATOM 1060 O ARG A 842 −17.800 31.737 −6.407 1.00 47.23 ATOM 1061 CB ARG A 842 −20.199 31.600 −4.533 1.00 50.08 ATOM 1062 CG ARG A 842 −21.388 32.452 −4.221 1.00 55.04 ATOM 1063 CD ARG A 842 −21.436 32.802 −2.759 1.00 59.44 ATOM 1064 NE ARG A 842 −22.511 33.746 −2.470 1.00 62.17 ATOM 1065 CZ ARG A 842 −22.698 34.317 −1.286 1.00 63.69 ATOM 1066 NH1 ARG A 842 −21.881 34.037 −0.282 1.00 65.35 ATOM 1067 NH2 ARG A 842 −23.699 35.166 −1.106 1.00 64.62 ATOM 1068 N ASP A 843 −18.349 29.568 −6.440 1.00 46.08 ATOM 1069 CA ASP A 843 −16.978 29.160 −6.714 1.00 44.50 ATOM 1070 C ASP A 843 −16.877 27.969 −7.671 1.00 42.28 ATOM 1071 O ASP A 843 −16.163 26.997 −7.412 1.00 39.78 ATOM 1072 CB ASP A 843 −16.260 28.857 −5.393 1.00 44.95 ATOM 1073 CG ASP A 843 −14.794 28.536 −5.588 1.00 45.84 ATOM 1074 OD1 ASP A 843 −14.145 29.230 −6.403 1.00 47.66 ATOM 1075 OD2 ASP A 843 −14.293 27.600 −4.925 1.00 44.46 ATOM 1076 N LEU A 844 −17.601 28.052 −8.781 1.00 39.91 ATOM 1077 CA LEU A 844 −17.569 26.997 −9.774 1.00 38.68 ATOM 1078 C LEU A 844 −16.267 27.143 −10.579 1.00 39.36 ATOM 1079 O LEU A 844 −15.909 28.244 −11.012 1.00 36.39 ATOM 1080 CB LEU A 844 −18.787 27.110 −10.690 1.00 37.44 ATOM 1081 CG LEU A 844 −18.818 26.190 −11.918 1.00 35.03 ATOM 1082 CD1 LEU A 844 −18.793 24.735 −11.502 1.00 33.46 ATOM 1083 CD2 LEU A 844 −20.061 26.486 −12.710 1.00 33.77 ATOM 1084 N ALA A 845 −15.554 26.035 −10.749 1.00 38.08 ATOM 1085 CA ALA A 845 −14.294 26.041 −11.481 1.00 41.74 ATOM 1086 C ALA A 845 −13.890 24.602 −11.766 1.00 43.66 ATOM 1087 O ALA A 845 −14.272 23.692 −11.029 1.00 45.06 ATOM 1088 CB ALA A 845 −13.209 26.740 −10.653 1.00 41.01 ATOM 1089 N ALA A 846 −13.128 24.388 −12.832 1.00 45.09 ATOM 1090 CA ALA A 846 −12.706 23.034 −13.183 1.00 46.69 ATOM 1091 C ALA A 846 −12.244 22.297 −11.933 1.00 47.45 ATOM 1092 O ALA A 846 −12.454 21.094 −11.789 1.00 49.65 ATOM 1093 CB ALA A 846 −11.591 23.083 −14.208 1.00 45.74 ATOM 1094 N ARG A 847 −11.632 23.047 −11.027 1.00 49.09 ATOM 1095 CA ARG A 847 −11.117 22.527 −9.759 1.00 50.53 ATOM 1096 C ARG A 847 −12.175 21.893 −8.858 1.00 50.50 ATOM 1097 O ARG A 847 −11.872 20.978 −8.100 1.00 51.14 ATOM 1098 CB ARG A 847 −10.421 23.664 −9.015 1.00 52.11 ATOM 1099 CG ARG A 847 −10.116 23.414 −7.567 1.00 55.22 ATOM 1100 CD ARG A 847 −9.438 24.635 −7.002 1.00 54.87 ATOM 1101 NE ARG A 847 −10.266 25.814 −7.214 1.00 59.60 ATOM 1102 CZ ARG A 847 −11.222 26.221 −6.381 1.00 62.29 ATOM 1103 NH1 ARG A 847 −11.468 25.543 −5.262 1.00 63.16 ATOM 1104 NH2 ARG A 847 −11.942 27.298 −6.676 1.00 61.26 ATOM 1105 N ASN A 848 −13.412 22.374 −8.931 1.00 49.43 ATOM 1106 CA ASN A 848 −14.469 21.819 −8.099 1.00 47.44 ATOM 1107 C ASN A 848 −15.438 20.903 −8.840 1.00 48.04 ATOM 1108 O ASN A 848 −16.612 20.784 −8.472 1.00 48.54 ATOM 1109 CB ASN A 848 −15.236 22.934 −7.384 1.00 45.48 ATOM 1110 CG ASN A 848 −14.397 23.628 −6.337 1.00 45.91 ATOM 1111 OD1 ASN A 848 −13.754 22.979 −5.521 1.00 50.11 ATOM 1112 ND2 ASN A 848 −14.406 24.950 −6.347 1.00 43.85 ATOM 1113 N VAL A 849 −14.951 20.265 −9.897 1.00 46.96 ATOM 1114 CA VAL A 849 −15.771 19.318 −10.637 1.00 47.48 ATOM 1115 C VAL A 849 −15.026 17.994 −10.477 1.00 48.51 ATOM 1116 O VAL A 849 −13.826 17.913 −10.729 1.00 49.29 ATOM 1117 CB VAL A 849 −15.896 19.688 −12.145 1.00 47.07 ATOM 1118 CG1 VAL A 849 −16.754 18.653 −12.871 1.00 47.56 ATOM 1119 CG2 VAL A 849 −16.517 21.065 −12.298 1.00 45.99 ATOM 1120 N LEU A 850 −15.730 16.965 −10.026 1.00 48.67 ATOM 1121 CA LEU A 850 −15.109 15.667 −9.813 1.00 47.31 ATOM 1122 C LEU A 850 −15.554 14.634 −10.855 1.00 48.46 ATOM 1123 O LEU A 850 −16.641 14.733 −11.430 1.00 47.00 ATOM 1124 CB LEU A 850 −15.437 15.165 −8.402 1.00 43.85 ATOM 1125 CG LEU A 850 −15.177 16.144 −7.255 1.00 42.97 ATOM 1126 CD1 LEU A 850 −15.709 15.561 −5.970 1.00 40.25 ATOM 1127 CD2 LEU A 850 −13.694 16.439 −7.137 1.00 42.26 ATOM 1128 N VAL A 851 −14.701 13.638 −11.082 1.00 50.16 ATOM 1129 CA VAL A 851 −14.985 12.588 −12.045 1.00 51.71 ATOM 1130 C VAL A 851 −15.343 11.257 −11.371 1.00 54.08 ATOM 1131 O VAL A 851 −14.485 10.615 −10.757 1.00 53.24 ATOM 1132 CB VAL A 851 −13.772 12.355 −12.963 1.00 51.18 ATOM 1133 CG1 VAL A 851 −14.208 11.572 −14.195 1.00 53.03 ATOM 1134 CG2 VAL A 851 −13.136 13.683 −13.351 1.00 48.08 ATOM 1135 N LYS A 852 −16.610 10.854 −11.473 1.00 56.51 ATOM 1136 CA LYS A 852 −17.060 9.581 −10.897 1.00 60.15 ATOM 1137 C LYS A 852 −16.552 8.520 −11.863 1.00 62.24 ATOM 1138 O LYS A 852 −16.067 7.461 −11.464 1.00 64.74 ATOM 1139 CB LYS A 852 −18.584 9.524 −10.829 1.00 60.47 ATOM 1140 CG LYS A 852 −19.156 8.246 −10.229 1.00 61.94 ATOM 1141 CD LYS A 852 −20.672 8.239 −10.404 1.00 66.23 ATOM 1142 CE LYS A 852 −21.375 7.079 −9.703 1.00 66.46 ATOM 1143 NZ LYS A 852 −22.871 7.181 −9.873 1.00 66.94 ATOM 1144 N SER A 853 −16.671 8.837 −13.145 1.00 62.50 ATOM 1145 CA SER A 853 −16.212 7.989 −14.233 1.00 62.66 ATOM 1146 C SER A 853 −16.012 8.924 −15.431 1.00 61.67 ATOM 1147 O SER A 853 −16.624 9.988 −15.499 1.00 60.83 ATOM 1148 CB SER A 853 −17.233 6.882 −14.536 1.00 63.56 ATOM 1149 OG SER A 853 −18.560 7.374 −14.594 1.00 66.67 ATOM 1150 N PRO A 854 −15.134 8.551 −16.373 1.00 60.36 ATOM 1151 CA PRO A 854 −14.849 9.364 −17.558 1.00 59.12 ATOM 1152 C PRO A 854 −16.065 10.032 −18.179 1.00 57.95 ATOM 1153 O PRO A 854 −16.003 11.182 −18.610 1.00 56.93 ATOM 1154 CB PRO A 854 −14.188 8.365 −18.500 1.00 60.62 ATOM 1155 CG PRO A 854 −13.413 7.508 −17.550 1.00 60.96 ATOM 1156 CD PRO A 854 −14.418 7.263 −16.443 1.00 61.47 ATOM 1157 N ALA A 855 −17.175 9.313 −18.210 1.00 56.59 ATOM 1158 CA ALA A 855 −18.391 9.842 −18.801 1.00 56.60 ATOM 1159 C ALA A 855 −19.414 10.316 −17.762 1.00 55.94 ATOM 1160 O ALA A 855 −20.605 10.376 −18.046 1.00 55.12 ATOM 1161 CB ALA A 855 −19.009 8.779 −19.699 1.00 57.53 ATOM 1162 N HIS A 856 −18.954 10.674 −16.568 1.00 55.98 ATOM 1163 CA HIS A 856 −19.869 11.100 −15.513 1.00 53.27 ATOM 1164 C HIS A 856 −19.169 11.954 −14.460 1.00 51.77 ATOM 1165 O HIS A 856 −18.433 11.446 −13.618 1.00 53.22 ATOM 1166 CB HIS A 856 −20.477 9.858 −14.858 1.00 54.21 ATOM 1167 CG HIS A 856 −21.564 10.146 −13.868 1.00 56.69 ATOM 1168 ND1 HIS A 856 −22.263 9.145 −13.227 1.00 56.79 ATOM 1169 CD2 HIS A 856 −22.080 11.312 −13.416 1.00 55.96 ATOM 1170 CE1 HIS A 856 −23.163 9.681 −12.425 1.00 57.20 ATOM 1171 NE2 HIS A 856 −23.073 10.995 −12.521 1.00 57.31 ATOM 1172 N VAL A 857 −19.397 13.259 −14.514 1.00 49.26 ATOM 1173 CA VAL A 857 −18.794 14.161 −13.550 1.00 46.76 ATOM 1174 C VAL A 857 −19.864 14.686 −12.589 1.00 46.86 ATOM 1175 O VAL A 857 −21.065 14.579 −12.861 1.00 46.96 ATOM 1176 CB VAL A 857 −18.058 15.343 −14.260 1.00 46.02 ATOM 1177 CG1 VAL A 857 −16.777 14.830 −14.928 1.00 41.78 ATOM 1178 CG2 VAL A 857 −18.961 15.992 −15.285 1.00 38.84 ATOM 1179 N LYS A 858 −19.422 15.226 −11.458 1.00 45.57 ATOM 1180 CA LYS A 858 −20.322 15.767 −10.437 1.00 45.68 ATOM 1181 C LYS A 858 −19.765 17.090 −9.923 1.00 45.10 ATOM 1182 O LYS A 858 −18.552 17.220 −9.727 1.00 43.10 ATOM 1183 CB LYS A 858 −20.442 14.804 −9.242 1.00 46.28 ATOM 1184 CG LYS A 858 −21.257 13.521 −9.451 1.00 45.72 ATOM 1185 CD LYS A 858 −21.160 12.646 −8.184 1.00 44.10 ATOM 1186 CE LYS A 858 −21.914 11.324 −8.292 1.00 45.25 ATOM 1187 NZ LYS A 858 −23.401 11.471 −8.255 1.00 47.27 ATOM 1188 N ILE A 859 −20.643 18.068 −9.703 1.00 45.57 ATOM 1189 CA ILE A 859 −20.203 19.363 −9.185 1.00 45.70 ATOM 1190 C ILE A 859 −20.098 19.256 −7.669 1.00 47.41 ATOM 1191 O ILE A 859 −20.981 18.687 −7.023 1.00 48.32 ATOM 1192 CB ILE A 859 −21.185 20.482 −9.547 1.00 44.76 ATOM 1193 CG1 ILE A 859 −21.259 20.622 −11.074 1.00 44.37 ATOM 1194 CG2 ILE A 859 −20.724 21.793 −8.916 1.00 44.21 ATOM 1195 CD1 ILE A 859 −22.156 21.719 −11.561 1.00 40.72 ATOM 1196 N THR A 860 −19.018 19.787 −7.104 1.00 46.98 ATOM 1197 CA THR A 860 −18.811 19.711 −5.662 1.00 47.63 ATOM 1198 C THR A 860 −18.467 21.050 −5.024 1.00 48.69 ATOM 1199 O THR A 860 −18.155 22.019 −5.711 1.00 49.80 ATOM 1200 CB THR A 860 −17.670 18.714 −5.308 1.00 46.89 ATOM 1201 OG1 THR A 860 −17.661 18.468 −3.897 1.00 45.80 ATOM 1202 CG2 THR A 860 −16.322 19.295 −5.686 1.00 44.93 ATOM 1203 N ASP A 861 −18.526 21.078 −3.696 1.00 49.00 ATOM 1204 CA ASP A 861 −18.195 22.253 −2.897 1.00 51.12 ATOM 1205 C ASP A 861 −19.116 23.454 −2.982 1.00 52.18 ATOM 1206 O ASP A 861 −18.722 24.560 −2.630 1.00 53.11 ATOM 1207 CB ASP A 861 −16.767 22.716 −3.177 1.00 49.84 ATOM 1208 CG ASP A 861 −16.057 23.146 −1.914 1.00 52.95 ATOM 1209 OD1 ASP A 861 −16.108 22.375 −0.941 1.00 55.50 ATOM 1210 OD2 ASP A 861 −15.451 24.233 −1.871 1.00 55.17 ATOM 1211 N PHE A 862 −20.340 23.254 −3.440 1.00 54.22 ATOM 1212 CA PHE A 862 −21.269 24.367 −3.500 1.00 57.56 ATOM 1213 C PHE A 862 −21.792 24.637 −2.080 1.00 61.09 ATOM 1214 O PHE A 862 −22.294 23.734 −1.410 1.00 62.23 ATOM 1215 CB PHE A 862 −22.429 24.032 −4.437 1.00 55.96 ATOM 1216 CG PHE A 862 −23.035 22.671 −4.197 1.00 55.99 ATOM 1217 CD1 PHE A 862 −22.751 21.609 −5.051 1.00 56.15 ATOM 1218 CD2 PHE A 862 −23.883 22.448 −3.115 1.00 53.52 ATOM 1219 CE1 PHE A 862 −23.302 20.348 −4.829 1.00 56.04 ATOM 1220 CE2 PHE A 862 −24.435 21.195 −2.886 1.00 52.92 ATOM 1221 CZ PHE A 862 −24.144 20.141 −3.746 1.00 54.63 ATOM 1222 N GLY A 863 −21.651 25.866 −1.600 1.00 64.10 ATOM 1223 CA GLY A 863 −22.153 26.162 −0.268 1.00 67.86 ATOM 1224 C GLY A 863 −21.176 26.776 0.716 1.00 70.52 ATOM 1225 O GLY A 863 −21.529 27.720 1.427 1.00 70.56 ATOM 1226 N LEU A 864 −19.959 26.240 0.780 1.00 72.06 ATOM 1227 CA LEU A 864 −18.953 26.772 1.691 1.00 73.84 ATOM 1228 C LEU A 864 −18.657 28.229 1.337 1.00 75.19 ATOM 1229 O LEU A 864 −18.297 29.027 2.199 1.00 77.44 ATOM 1230 CB LEU A 864 −17.660 25.955 1.610 1.00 73.25 ATOM 1231 CG LEU A 864 −17.786 24.442 1.773 1.00 72.21 ATOM 1232 CD1 LEU A 864 −16.405 23.833 1.808 1.00 71.56 ATOM 1233 CD2 LEU A 864 −18.543 24.115 3.037 1.00 71.95 ATOM 1234 N ALA A 865 −18.812 28.569 0.064 1.00 75.54 ATOM 1235 CA ALA A 865 −18.564 29.924 −0.403 1.00 75.51 ATOM 1236 C ALA A 865 −19.274 30.937 0.485 1.00 76.03 ATOM 1237 O ALA A 865 −18.654 31.859 1.020 1.00 77.18 ATOM 1238 CB ALA A 865 −19.048 30.067 −1.834 1.00 76.59 ATOM 1239 N ARG A 866 −20.579 30.757 0.641 1.00 75.54 ATOM 1240 CA ARG A 866 −21.389 31.661 1.448 1.00 74.65 ATOM 1241 C ARG A 866 −21.168 31.435 2.940 1.00 73.26 ATOM 1242 O ARG A 866 −21.048 32.382 3.716 1.00 72.57 ATOM 1243 CB ARG A 866 −22.869 31.456 1.116 1.00 75.86 ATOM 1244 CG ARG A 866 −23.797 32.543 1.621 1.00 78.29 ATOM 1245 CD ARG A 866 −25.223 32.212 1.231 1.00 81.93 ATOM 1246 NE ARG A 866 −26.098 33.379 1.227 1.00 85.05 ATOM 1247 CZ ARG A 866 −27.359 33.362 0.800 1.00 87.00 ATOM 1248 NH1 ARG A 866 −27.893 32.233 0.343 1.00 86.94 ATOM 1249 NH2 ARG A 866 −28.082 34.476 0.816 1.00 88.11 ATOM 1250 N LEU A 867 −21.104 30.172 3.333 1.00 71.68 ATOM 1251 CA LEU A 867 −20.929 29.817 4.732 1.00 71.24 ATOM 1252 C LEU A 867 −19.657 30.365 5.369 1.00 70.68 ATOM 1253 O LEU A 867 −19.642 30.649 6.566 1.00 70.39 ATOM 1254 CB LEU A 867 −20.963 28.296 4.885 1.00 70.78 ATOM 1255 CG LEU A 867 −21.160 27.766 6.300 1.00 69.00 ATOM 1256 CD1 LEU A 867 −22.544 28.150 6.800 1.00 70.14 ATOM 1257 CD2 LEU A 867 −21.006 26.262 6.299 1.00 69.35 ATOM 1258 N LEU A 868 −18.597 30.519 4.579 1.00 70.51 ATOM 1259 CA LEU A 868 −17.333 31.021 5.108 1.00 70.64 ATOM 1260 C LEU A 868 −17.202 32.537 5.032 1.00 71.18 ATOM 1261 O LEU A 868 −16.786 33.179 5.996 1.00 71.59 ATOM 1262 CB LEU A 868 −16.152 30.362 4.390 1.00 70.84 ATOM 1263 CG LEU A 868 −16.175 28.826 4.286 1.00 72.40 ATOM 1264 CD1 LEU A 868 −14.780 28.326 3.889 1.00 70.82 ATOM 1265 CD2 LEU A 868 −16.614 28.201 5.610 1.00 70.35 ATOM 1266 N GLU A 869 −17.549 33.121 3.894 1.00 72.14 ATOM 1267 CA GLU A 869 −17.456 34.567 3.771 1.00 72.99 ATOM 1268 C GLU A 869 −18.658 35.262 4.389 1.00 72.22 ATOM 1269 O GLU A 869 −18.633 35.645 5.558 1.00 72.77 ATOM 1270 CB GLU A 869 −17.316 34.968 2.311 1.00 74.69 ATOM 1271 CG GLU A 869 −15.925 34.742 1.782 1.00 78.22 ATOM 1272 CD GLU A 869 −15.688 35.427 0.451 1.00 81.09 ATOM 1273 OE1 GLU A 869 −14.505 35.593 0.097 1.00 81.80 ATOM 1274 OE2 GLU A 869 −16.671 35.793 −0.241 1.00 81.14 ATOM 1275 N GLY A 870 −19.713 35.415 3.602 1.00 71.14 ATOM 1276 CA GLY A 870 −20.910 36.064 4.093 1.00 69.73 ATOM 1277 C GLY A 870 −21.585 36.758 2.941 1.00 69.34 ATOM 1278 O GLY A 870 −21.266 36.488 1.788 1.00 67.87 ATOM 1279 N ASP A 871 −22.514 37.654 3.245 1.00 70.63 ATOM 1280 CA ASP A 871 −23.221 38.388 2.206 1.00 71.41 ATOM 1281 C ASP A 871 −22.979 39.888 2.287 1.00 69.67 ATOM 1282 O ASP A 871 −23.710 40.673 1.693 1.00 70.04 ATOM 1283 CB ASP A 871 −24.720 38.092 2.291 1.00 75.78 ATOM 1284 CG ASP A 871 −25.081 36.742 1.692 1.00 80.13 ATOM 1285 OD1 ASP A 871 −25.017 36.611 0.448 1.00 82.71 ATOM 1286 OD2 ASP A 871 −25.419 35.811 2.458 1.00 81.77 ATOM 1287 N GLU A 872 −21.945 40.288 3.018 1.00 69.40 ATOM 1288 CA GLU A 872 −21.638 41.704 3.156 1.00 69.92 ATOM 1289 C GLU A 872 −21.292 42.261 1.783 1.00 67.97 ATOM 1290 O GLU A 872 −20.261 41.926 1.204 1.00 67.08 ATOM 1291 CB GLU A 872 −20.469 41.902 4.125 1.00 72.87 ATOM 1292 CG GLU A 872 −20.340 43.319 4.675 1.00 78.70 ATOM 1293 CD GLU A 872 −19.204 43.458 5.689 1.00 83.05 ATOM 1294 OE1 GLU A 872 −19.079 44.535 6.318 1.00 83.94 ATOM 1295 OE2 GLU A 872 −18.429 42.490 5.857 1.00 86.32 ATOM 1296 N LYS A 873 −22.169 43.109 1.264 1.00 66.05 ATOM 1297 CA LYS A 873 −21.976 43.703 −0.046 1.00 65.17 ATOM 1298 C LYS A 873 −20.551 44.188 −0.314 1.00 64.82 ATOM 1299 O LYS A 873 −19.998 43.941 −1.380 1.00 64.23 ATOM 1300 CB LYS A 873 −22.956 44.864 −0.234 1.00 65.59 ATOM 1301 CG LYS A 873 −22.803 45.611 −1.561 1.00 68.09 ATOM 1302 CD LYS A 873 −23.875 46.686 −1.729 1.00 69.73 ATOM 1303 CE LYS A 873 −23.672 47.499 −3.007 1.00 71.60 ATOM 1304 NZ LYS A 873 −24.749 48.517 −3.211 1.00 71.19 ATOM 1305 N GLU A 874 −19.949 44.873 0.652 1.00 65.02 ATOM 1306 CA GLU A 874 −18.603 45.397 0.454 1.00 63.95 ATOM 1307 C GLU A 874 −17.487 44.565 1.065 1.00 62.00 ATOM 1308 O GLU A 874 −17.587 44.080 2.194 1.00 62.31 ATOM 1309 CB GLU A 874 −18.518 46.840 0.964 1.00 65.71 ATOM 1310 CG GLU A 874 −19.059 47.045 2.363 1.00 69.44 ATOM 1311 CD GLU A 874 −20.576 46.946 2.437 1.00 71.62 ATOM 1312 OE1 GLU A 874 −21.259 47.887 1.973 1.00 71.73 ATOM 1313 OE2 GLU A 874 −21.083 45.923 2.955 1.00 72.76 ATOM 1314 N TYR A 875 −16.422 44.399 0.290 1.00 59.06 ATOM 1315 CA TYR A 875 −15.259 43.641 0.720 1.00 57.62 ATOM 1316 C TYR A 875 −14.381 44.522 1.587 1.00 57.53 ATOM 1317 O TYR A 875 −14.266 45.724 1.349 1.00 56.84 ATOM 1318 CB TYR A 875 −14.414 43.225 −0.480 1.00 56.65 ATOM 1319 CG TYR A 875 −15.098 42.342 −1.484 1.00 56.70 ATOM 1320 CD1 TYR A 875 −15.421 41.027 −1.173 1.00 56.15 ATOM 1321 CD2 TYR A 875 −15.402 42.817 −2.759 1.00 55.46 ATOM 1322 CE1 TYR A 875 −16.027 40.205 −2.103 1.00 56.63 ATOM 1323 CE2 TYR A 875 −16.007 42.005 −3.697 1.00 55.93 ATOM 1324 CZ TYR A 875 −16.319 40.697 −3.362 1.00 56.44 ATOM 1325 OH TYR A 875 −16.933 39.879 −4.275 1.00 55.10 ATOM 1326 N ASN A 876 −13.760 43.933 2.597 1.00 57.67 ATOM 1327 CA ASN A 876 −12.852 44.705 3.409 1.00 58.46 ATOM 1328 C ASN A 876 −11.471 44.340 2.859 1.00 59.52 ATOM 1329 O ASN A 876 −11.382 43.709 1.806 1.00 58.53 ATOM 1330 CB ASN A 876 −13.016 44.393 4.908 1.00 59.97 ATOM 1331 CG ASN A 876 −12.785 42.934 5.255 1.00 63.94 ATOM 1332 OD1 ASN A 876 −11.833 42.311 4.775 1.00 67.34 ATOM 1333 ND2 ASN A 876 −13.642 42.387 6.125 1.00 61.21 ATOM 1334 N ALA A 877 −10.405 44.736 3.546 1.00 60.79 ATOM 1335 CA ALA A 877 −9.041 44.483 3.081 1.00 61.10 ATOM 1336 C ALA A 877 −8.689 43.019 2.829 1.00 62.40 ATOM 1337 O ALA A 877 −7.782 42.714 2.046 1.00 61.52 ATOM 1338 CB ALA A 877 −8.058 45.080 4.066 1.00 60.97 ATOM 1339 N ASP A 878 −9.409 42.122 3.494 1.00 63.27 ATOM 1340 CA ASP A 878 −9.172 40.690 3.370 1.00 63.19 ATOM 1341 C ASP A 878 −9.636 40.145 2.022 1.00 63.64 ATOM 1342 O ASP A 878 −9.158 39.107 1.569 1.00 63.47 ATOM 1343 CB ASP A 878 −9.879 39.958 4.509 1.00 62.08 ATOM 1344 CG ASP A 878 −9.278 38.604 4.787 1.00 64.16 ATOM 1345 OD1 ASP A 878 −8.034 38.520 4.917 1.00 63.46 ATOM 1346 OD2 ASP A 878 −10.047 37.624 4.885 1.00 65.45 ATOM 1347 N GLY A 879 −10.571 40.848 1.387 1.00 64.96 ATOM 1348 CA GLY A 879 −11.081 40.422 0.092 1.00 66.39 ATOM 1349 C GLY A 879 −11.894 39.139 0.105 1.00 66.47 ATOM 1350 O GLY A 879 −12.483 38.779 1.124 1.00 67.04 ATOM 1351 N GLY A 880 −11.920 38.443 −1.031 1.00 66.80 ATOM 1352 CA GLY A 880 −12.676 37.204 −1.127 1.00 66.89 ATOM 1353 C GLY A 880 −11.850 35.931 −1.217 1.00 66.50 ATOM 1354 O GLY A 880 −10.679 35.976 −1.586 1.00 67.73 ATOM 1355 N LYS A 881 −12.461 34.793 −0.892 1.00 66.57 ATOM 1356 CA LYS A 881 −11.773 33.503 −0.935 1.00 67.51 ATOM 1357 C LYS A 881 −11.804 32.841 −2.316 1.00 66.54 ATOM 1358 O LYS A 881 −10.988 31.958 −2.597 1.00 66.96 ATOM 1359 CB LYS A 881 −12.353 32.538 0.116 1.00 69.38 ATOM 1360 CG LYS A 881 −12.196 33.032 1.552 1.00 73.80 ATOM 1361 CD LYS A 881 −12.514 31.966 2.608 1.00 76.95 ATOM 1362 CE LYS A 881 −12.271 32.525 4.032 1.00 79.84 ATOM 1363 NZ LYS A 881 −12.387 31.531 5.153 1.00 77.75 ATOM 1364 N MET A 882 −12.738 33.255 −3.172 1.00 63.86 ATOM 1365 CA MET A 882 −12.822 32.682 −4.512 1.00 62.87 ATOM 1366 C MET A 882 −11.752 33.268 −5.420 1.00 59.24 ATOM 1367 O MET A 882 −11.448 34.453 −5.344 1.00 59.24 ATOM 1368 CB MET A 882 −14.182 32.957 −5.152 1.00 67.37 ATOM 1369 CG MET A 882 −15.308 32.094 −4.663 1.00 73.66 ATOM 1370 SD MET A 882 −15.853 32.567 −3.040 1.00 80.15 ATOM 1371 CE MET A 882 −15.822 30.977 −2.239 1.00 79.51 ATOM 1372 N PRO A 883 −11.175 32.447 −6.303 1.00 55.61 ATOM 1373 CA PRO A 883 −10.150 33.005 −7.180 1.00 54.96 ATOM 1374 C PRO A 883 −10.749 34.048 −8.127 1.00 54.82 ATOM 1375 O PRO A 883 −11.750 33.794 −8.788 1.00 54.42 ATOM 1376 CB PRO A 883 −9.598 31.769 −7.892 1.00 54.93 ATOM 1377 CG PRO A 883 −10.765 30.818 −7.897 1.00 55.39 ATOM 1378 CD PRO A 883 −11.367 31.006 −6.539 1.00 54.78 ATOM 1379 N ILE A 884 −10.122 35.221 −8.166 1.00 55.44 ATOM 1380 CA ILE A 884 −10.536 36.360 −8.986 1.00 55.16 ATOM 1381 C ILE A 884 −10.812 36.062 −10.462 1.00 54.77 ATOM 1382 O ILE A 884 −11.743 36.609 −11.052 1.00 54.35 ATOM 1383 CB ILE A 884 −9.457 37.490 −8.930 1.00 57.82 ATOM 1384 CG1 ILE A 884 −9.280 37.996 −7.492 1.00 60.91 ATOM 1385 CG2 ILE A 884 −9.863 38.658 −9.812 1.00 57.84 ATOM 1386 CD1 ILE A 884 −10.456 38.817 −6.963 1.00 61.63 ATOM 1387 N LYS A 885 −10.003 35.196 −11.057 1.00 54.04 ATOM 1388 CA LYS A 885 −10.126 34.878 −12.476 1.00 53.74 ATOM 1389 C LYS A 885 −11.342 34.054 −12.922 1.00 52.87 ATOM 1390 O LYS A 885 −11.586 33.890 −14.117 1.00 53.63 ATOM 1391 CB LYS A 885 −8.823 34.222 −12.937 1.00 55.38 ATOM 1392 CG LYS A 885 −7.609 35.112 −12.690 1.00 57.08 ATOM 1393 CD LYS A 885 −6.308 34.437 −13.069 1.00 59.92 ATOM 1394 CE LYS A 885 −5.131 35.372 −12.845 1.00 62.00 ATOM 1395 NZ LYS A 885 −3.829 34.700 −13.114 1.00 65.60 ATOM 1396 N TRP A 886 −12.108 33.546 −11.967 1.00 50.16 ATOM 1397 CA TRP A 886 −13.304 32.766 −12.271 1.00 47.41 ATOM 1398 C TRP A 886 −14.526 33.578 −11.836 1.00 47.34 ATOM 1399 O TRP A 886 −15.664 33.109 −11.882 1.00 47.47 ATOM 1400 CB TRP A 886 −13.268 31.461 −11.483 1.00 45.53 ATOM 1401 CG TRP A 886 −12.483 30.373 −12.121 1.00 45.12 ATOM 1402 CD1 TRP A 886 −12.967 29.373 −12.911 1.00 42.75 ATOM 1403 CD2 TRP A 886 −11.077 30.149 −12.004 1.00 44.61 ATOM 1404 NE1 TRP A 886 −11.952 28.536 −13.288 1.00 42.27 ATOM 1405 CE2 TRP A 886 −10.778 28.989 −12.747 1.00 43.80 ATOM 1406 CE3 TRP A 886 −10.038 30.814 −11.344 1.00 45.37 ATOM 1407 CZ2 TRP A 886 −9.477 28.476 −12.850 1.00 41.96 ATOM 1408 CZ3 TRP A 886 −8.743 30.302 −11.448 1.00 45.18 ATOM 1409 CH2 TRP A 886 −8.478 29.144 −12.197 1.00 40.59 ATOM 1410 N MET A 887 −14.266 34.809 −11.428 1.00 45.49 ATOM 1411 CA MET A 887 −15.292 35.689 −10.903 1.00 47.92 ATOM 1412 C MET A 887 −15.945 36.606 −11.924 1.00 47.15 ATOM 1413 O MET A 887 −15.286 37.112 −12.826 1.00 46.97 ATOM 1414 CB MET A 887 −14.655 36.521 −9.781 1.00 50.44 ATOM 1415 CG MET A 887 −15.580 37.050 −8.724 1.00 51.18 ATOM 1416 SD MET A 887 −14.641 37.374 −7.213 1.00 53.31 ATOM 1417 CE MET A 887 −14.838 35.821 −6.359 1.00 55.22 ATOM 1418 N ALA A 888 −17.248 36.814 −11.771 1.00 46.65 ATOM 1419 CA ALA A 888 −17.992 37.707 −12.653 1.00 47.77 ATOM 1420 C ALA A 888 −17.620 39.138 −12.281 1.00 48.61 ATOM 1421 O ALA A 888 −17.515 39.483 −11.104 1.00 48.25 ATOM 1422 CB ALA A 888 −19.491 37.497 −12.486 1.00 45.93 ATOM 1423 N LEU A 889 −17.418 39.965 −13.294 1.00 50.52 ATOM 1424 CA LEU A 889 −17.030 41.350 −13.098 1.00 51.06 ATOM 1425 C LEU A 889 −17.751 42.039 −11.953 1.00 52.52 ATOM 1426 O LEU A 889 −17.122 42.682 −11.104 1.00 52.90 ATOM 1427 CB LEU A 889 −17.270 42.121 −14.387 1.00 52.30 ATOM 1428 CG LEU A 889 −16.926 43.607 −14.399 1.00 53.28 ATOM 1429 CD1 LEU A 889 −15.502 43.802 −13.915 1.00 53.95 ATOM 1430 CD2 LEU A 889 −17.114 44.154 −15.816 1.00 49.72 ATOM 1431 N GLU A 890 −19.072 41.894 −11.919 1.00 52.25 ATOM 1432 CA GLU A 890 −19.864 42.538 −10.881 1.00 52.51 ATOM 1433 C GLU A 890 −19.517 42.070 −9.482 1.00 54.25 ATOM 1434 O GLU A 890 −19.668 42.821 −8.520 1.00 55.68 ATOM 1435 CB GLU A 890 −21.361 42.322 −11.116 1.00 51.54 ATOM 1436 CG GLU A 890 −21.799 40.871 −11.075 1.00 49.82 ATOM 1437 CD GLU A 890 −21.820 40.236 −12.448 1.00 47.38 ATOM 1438 OE1 GLU A 890 −20.989 40.647 −13.299 1.00 40.49 ATOM 1439 OE2 GLU A 890 −22.664 39.326 −12.650 1.00 42.65 ATOM 1440 N CYS A 891 −19.059 40.832 −9.361 1.00 55.67 ATOM 1441 CA CYS A 891 −18.720 40.296 −8.052 1.00 56.74 ATOM 1442 C CYS A 891 −17.300 40.649 −7.605 1.00 57.48 ATOM 1443 O CYS A 891 −16.868 40.297 −6.508 1.00 55.50 ATOM 1444 CB CYS A 891 −18.956 38.781 −8.036 1.00 57.62 ATOM 1445 SG CYS A 891 −20.729 38.333 −7.970 1.00 57.17 ATOM 1446 N ILE A 892 −16.576 41.362 −8.458 1.00 58.80 ATOM 1447 CA ILE A 892 −15.224 41.780 −8.112 1.00 59.01 ATOM 1448 C ILE A 892 −15.285 43.087 −7.319 1.00 59.18 ATOM 1449 O ILE A 892 −14.529 43.274 −6.374 1.00 60.68 ATOM 1450 CB ILE A 892 −14.357 42.018 −9.369 1.00 57.56 ATOM 1451 CG1 ILE A 892 −14.003 40.684 −10.024 1.00 56.20 ATOM 1452 CG2 ILE A 892 −13.104 42.792 −8.996 1.00 54.39 ATOM 1453 CD1 ILE A 892 −13.252 40.841 −11.323 1.00 56.41 ATOM 1454 N HIS A 893 −16.193 43.981 −7.707 1.00 58.73 ATOM 1455 CA HIS A 893 −16.333 45.274 −7.046 1.00 57.13 ATOM 1456 C HIS A 893 −17.139 45.236 −5.757 1.00 55.23 ATOM 1457 O HIS A 893 −16.951 46.075 −4.879 1.00 55.68 ATOM 1458 CB HIS A 893 −16.947 46.276 −8.015 1.00 58.88 ATOM 1459 CG HIS A 893 −16.103 46.532 −9.225 1.00 62.09 ATOM 1460 ND1 HIS A 893 −16.555 46.318 −10.510 1.00 62.92 ATOM 1461 CD2 HIS A 893 −14.825 46.969 −9.344 1.00 63.01 ATOM 1462 CE1 HIS A 893 −15.593 46.609 −11.368 1.00 63.20 ATOM 1463 NE2 HIS A 893 −14.532 47.006 −10.687 1.00 63.80 ATOM 1464 N TYR A 894 −18.031 44.258 −5.652 1.00 53.00 ATOM 1465 CA TYR A 894 −18.887 44.072 −4.477 1.00 51.14 ATOM 1466 C TYR A 894 −19.364 42.639 −4.549 1.00 49.31 ATOM 1467 O TYR A 894 −19.093 41.949 −5.518 1.00 50.31 ATOM 1468 CB TYR A 894 −20.135 44.959 −4.542 1.00 52.50 ATOM 1469 CG TYR A 894 −19.895 46.444 −4.526 1.00 53.58 ATOM 1470 CD1 TYR A 894 −19.719 47.126 −3.327 1.00 54.62 ATOM 1471 CD2 TYR A 894 −19.832 47.167 −5.716 1.00 52.84 ATOM 1472 CE1 TYR A 894 −19.483 48.491 −3.313 1.00 57.08 ATOM 1473 CE2 TYR A 894 −19.594 48.529 −5.718 1.00 54.76 ATOM 1474 CZ TYR A 894 −19.417 49.190 −4.515 1.00 57.74 ATOM 1475 OH TYR A 894 −19.147 50.546 −4.505 1.00 59.64 ATOM 1476 N ARG A 895 −20.087 42.195 −3.534 1.00 48.76 ATOM 1477 CA ARG A 895 −20.624 40.845 −3.535 1.00 50.39 ATOM 1478 C ARG A 895 −22.022 40.867 −4.152 1.00 50.91 ATOM 1479 O ARG A 895 −23.002 41.194 −3.486 1.00 51.94 ATOM 1480 CB ARG A 895 −20.712 40.281 −2.112 1.00 49.62 ATOM 1481 CG ARG A 895 −19.382 39.914 −1.498 1.00 49.55 ATOM 1482 CD ARG A 895 −19.526 38.808 −0.460 1.00 49.12 ATOM 1483 NE ARG A 895 −18.216 38.395 0.034 1.00 53.76 ATOM 1484 CZ ARG A 895 −17.475 39.124 0.866 1.00 56.50 ATOM 1485 NH1 ARG A 895 −16.284 38.688 1.268 1.00 52.02 ATOM 1486 NH2 ARG A 895 −17.940 40.288 1.316 1.00 57.79 ATOM 1487 N ALA A 896 −22.109 40.534 −5.432 1.00 51.10 ATOM 1488 CA ALA A 896 −23.392 40.505 −6.122 1.00 49.65 ATOM 1489 C ALA A 896 −23.571 39.101 −6.670 1.00 47.43 ATOM 1490 O ALA A 896 −23.849 38.925 −7.843 1.00 46.98 ATOM 1491 CB ALA A 896 −23.405 41.530 −7.266 1.00 49.62 ATOM 1492 N PHE A 897 −23.417 38.098 −5.816 1.00 46.40 ATOM 1493 CA PHE A 897 −23.540 36.721 −6.276 1.00 46.89 ATOM 1494 C PHE A 897 −24.943 36.276 −6.689 1.00 45.30 ATOM 1495 O PHE A 897 −25.889 36.296 −5.902 1.00 44.45 ATOM 1496 CB PHE A 897 −22.965 35.759 −5.231 1.00 47.33 ATOM 1497 CG PHE A 897 −21.487 35.887 −5.058 1.00 48.54 ATOM 1498 CD1 PHE A 897 −20.952 36.469 −3.909 1.00 51.22 ATOM 1499 CD2 PHE A 897 −20.622 35.458 −6.061 1.00 49.59 ATOM 1500 CE1 PHE A 897 −19.567 36.627 −3.764 1.00 50.13 ATOM 1501 CE2 PHE A 897 −19.239 35.607 −5.932 1.00 49.10 ATOM 1502 CZ PHE A 897 −18.709 36.194 −4.780 1.00 50.78 ATOM 1503 N THR A 898 −25.055 35.867 −7.946 1.00 44.73 ATOM 1504 CA THR A 898 −26.324 35.413 −8.499 1.00 44.26 ATOM 1505 C THR A 898 −26.085 34.245 −9.422 1.00 43.33 ATOM 1506 O THR A 898 −24.942 33.943 −9.774 1.00 42.13 ATOM 1507 CB THR A 898 −27.000 36.497 −9.356 1.00 44.01 ATOM 1508 OG1 THR A 898 −26.211 36.730 −10.529 1.00 43.71 ATOM 1509 CG2 THR A 898 −27.148 37.786 −8.571 1.00 44.17 ATOM 1510 N HIS A 899 −27.171 33.595 −9.821 1.00 41.98 ATOM 1511 CA HIS A 899 −27.065 32.487 −10.748 1.00 42.31 ATOM 1512 C HIS A 899 −26.317 32.987 −11.982 1.00 41.21 ATOM 1513 O HIS A 899 −25.520 32.255 −12.567 1.00 42.33 ATOM 1514 CB HIS A 899 −28.457 31.985 −11.113 1.00 43.29 ATOM 1515 CG HIS A 899 −29.246 31.542 −9.927 1.00 45.33 ATOM 1516 ND1 HIS A 899 −28.795 30.571 −9.057 1.00 47.28 ATOM 1517 CD2 HIS A 899 −30.433 31.968 −9.435 1.00 46.03 ATOM 1518 CE1 HIS A 899 −29.667 30.418 −8.078 1.00 46.75 ATOM 1519 NE2 HIS A 899 −30.670 31.255 −8.283 1.00 49.17 ATOM 1520 N GLN A 900 −26.540 34.243 −12.358 1.00 39.59 ATOM 1521 CA GLN A 900 −25.842 34.776 −13.521 1.00 40.74 ATOM 1522 C GLN A 900 −24.325 34.960 −13.315 1.00 39.29 ATOM 1523 O GLN A 900 −23.565 34.901 −14.276 1.00 37.94 ATOM 1524 CB GLN A 900 −26.497 36.078 −14.002 1.00 40.33 ATOM 1525 CG GLN A 900 −27.937 35.893 −14.495 1.00 44.02 ATOM 1526 CD GLN A 900 −28.125 34.695 −15.443 1.00 47.54 ATOM 1527 OE1 GLN A 900 −28.722 33.677 −15.084 1.00 51.69 ATOM 1528 NE2 GLN A 900 −27.610 34.822 −16.660 1.00 48.77 ATOM 1529 N SER A 901 −23.869 35.171 −12.084 1.00 38.33 ATOM 1530 CA SER A 901 −22.428 35.303 −11.870 1.00 37.53 ATOM 1531 C SER A 901 −21.856 33.895 −12.004 1.00 40.00 ATOM 1532 O SER A 901 −20.757 33.702 −12.542 1.00 39.46 ATOM 1533 CB SER A 901 −22.116 35.891 −10.492 1.00 36.74 ATOM 1534 OG SER A 901 −22.775 35.195 −9.451 1.00 40.58 ATOM 1535 N ASP A 902 −22.626 32.913 −11.527 1.00 39.02 ATOM 1536 CA ASP A 902 −22.247 31.511 −11.623 1.00 37.25 ATOM 1537 C ASP A 902 −22.061 31.163 −13.110 1.00 37.82 ATOM 1538 O ASP A 902 −21.139 30.436 −13.480 1.00 37.20 ATOM 1539 CB ASP A 902 −23.337 30.624 −11.005 1.00 38.66 ATOM 1540 CG ASP A 902 −23.065 30.279 −9.533 1.00 40.83 ATOM 1541 OD1 ASP A 902 −22.241 30.958 −8.896 1.00 41.45 ATOM 1542 OD2 ASP A 902 −23.682 29.326 −9.004 1.00 42.94 ATOM 1543 N VAL A 903 −22.929 31.694 −13.966 1.00 36.71 ATOM 1544 CA VAL A 903 −22.819 31.414 −15.390 1.00 37.25 ATOM 1545 C VAL A 903 −21.473 31.890 −15.932 1.00 37.89 ATOM 1546 O VAL A 903 −20.866 31.234 −16.788 1.00 35.97 ATOM 1547 CB VAL A 903 −23.960 32.075 −16.191 1.00 37.16 ATOM 1548 CG1 VAL A 903 −23.578 32.159 −17.657 1.00 35.90 ATOM 1549 CG2 VAL A 903 −25.232 31.264 −16.043 1.00 34.45 ATOM 1550 N TRP A 904 −21.013 33.035 −15.435 1.00 38.74 ATOM 1551 CA TRP A 904 −19.722 33.574 −15.845 1.00 37.48 ATOM 1552 C TRP A 904 −18.660 32.523 −15.494 1.00 35.96 ATOM 1553 O TRP A 904 −17.845 32.134 −16.323 1.00 33.79 ATOM 1554 CB TRP A 904 −19.426 34.875 −15.084 1.00 39.00 ATOM 1555 CG TRP A 904 −18.094 35.469 −15.435 1.00 41.83 ATOM 1556 CD1 TRP A 904 −16.870 34.876 −15.304 1.00 40.23 ATOM 1557 CD2 TRP A 904 −17.858 36.746 −16.041 1.00 43.43 ATOM 1558 NE1 TRP A 904 −15.891 35.695 −15.799 1.00 41.66 ATOM 1559 CE2 TRP A 904 −16.464 36.853 −16.255 1.00 44.01 ATOM 1560 CE3 TRP A 904 −18.688 37.810 −16.425 1.00 44.89 ATOM 1561 CZ2 TRP A 904 −15.876 37.989 −16.840 1.00 45.74 ATOM 1562 CZ3 TRP A 904 −18.105 38.943 −17.010 1.00 46.53 ATOM 1563 CH2 TRP A 904 −16.710 39.020 −17.210 1.00 46.91 ATOM 1564 N SER A 905 −18.681 32.070 −14.249 1.00 34.90 ATOM 1565 CA SER A 905 −17.731 31.078 −13.794 1.00 38.24 ATOM 1566 C SER A 905 −17.793 29.865 −14.726 1.00 38.83 ATOM 1567 O SER A 905 −16.773 29.409 −15.250 1.00 41.08 ATOM 1568 CB SER A 905 −18.059 30.690 −12.354 1.00 39.02 ATOM 1569 OG SER A 905 −18.186 31.852 −11.545 1.00 39.18 ATOM 1570 N TYR A 906 −19.000 29.361 −14.935 1.00 38.14 ATOM 1571 CA TYR A 906 −19.231 28.233 −15.825 1.00 36.99 ATOM 1572 C TYR A 906 −18.456 28.460 −17.123 1.00 37.89 ATOM 1573 O TYR A 906 −17.770 27.574 −17.620 1.00 37.22 ATOM 1574 CB TYR A 906 −20.727 28.127 −16.130 1.00 37.09 ATOM 1575 CG TYR A 906 −21.060 27.090 −17.169 1.00 36.26 ATOM 1576 CD1 TYR A 906 −21.299 25.767 −16.809 1.00 33.65 ATOM 1577 CD2 TYR A 906 −21.056 27.421 −18.522 1.00 35.93 ATOM 1578 CE1 TYR A 906 −21.513 24.800 −17.765 1.00 35.24 ATOM 1579 CE2 TYR A 906 −21.269 26.461 −19.488 1.00 36.62 ATOM 1580 CZ TYR A 906 −21.494 25.147 −19.108 1.00 35.06 ATOM 1581 OH TYR A 906 −21.659 24.187 −20.077 1.00 32.16 ATOM 1582 N GLY A 907 −18.585 29.658 −17.677 1.00 38.18 ATOM 1583 CA GLY A 907 −17.866 29.974 −18.890 1.00 37.34 ATOM 1584 C GLY A 907 −16.368 29.758 −18.734 1.00 39.60 ATOM 1585 O GLY A 907 −15.749 29.097 −19.583 1.00 39.30 ATOM 1586 N VAL A 908 −15.775 30.294 −17.662 1.00 38.75 ATOM 1587 CA VAL A 908 −14.329 30.144 −17.460 1.00 37.84 ATOM 1588 C VAL A 908 −14.006 28.678 −17.254 1.00 38.99 ATOM 1589 O VAL A 908 −12.948 28.189 −17.669 1.00 38.75 ATOM 1590 CB VAL A 908 −13.810 30.938 −16.233 1.00 38.62 ATOM 1591 CG1 VAL A 908 −12.282 30.912 −16.209 1.00 35.04 ATOM 1592 CG2 VAL A 908 −14.315 32.372 −16.274 1.00 33.97 ATOM 1593 N THR A 909 −14.939 27.974 −16.627 1.00 38.38 ATOM 1594 CA THR A 909 −14.764 26.552 −16.375 1.00 37.41 ATOM 1595 C THR A 909 −14.710 25.688 −17.629 1.00 37.98 ATOM 1596 O THR A 909 −13.837 24.837 −17.747 1.00 39.71 ATOM 1597 CB THR A 909 −15.861 26.011 −15.472 1.00 34.91 ATOM 1598 OG1 THR A 909 −15.866 26.753 −14.253 1.00 33.91 ATOM 1599 CG2 THR A 909 −15.610 24.541 −15.161 1.00 34.30 ATOM 1600 N ILE A 910 −15.629 25.877 −18.569 1.00 38.77 ATOM 1601 CA ILE A 910 −15.566 25.043 −19.765 1.00 41.06 ATOM 1602 C ILE A 910 −14.357 25.445 −20.598 1.00 42.01 ATOM 1603 O ILE A 910 −13.887 24.676 −21.444 1.00 39.07 ATOM 1604 CB ILE A 910 −16.841 25.128 −20.628 1.00 40.40 ATOM 1605 CG1 ILE A 910 −17.064 26.549 −21.124 1.00 42.79 ATOM 1606 CG2 ILE A 910 −18.022 24.642 −19.822 1.00 43.12 ATOM 1607 CD1 ILE A 910 −18.166 26.673 −22.162 1.00 43.99 ATOM 1608 N TRP A 911 −13.857 26.656 −20.347 1.00 42.81 ATOM 1609 CA TRP A 911 −12.689 27.146 −21.052 1.00 43.02 ATOM 1610 C TRP A 911 −11.482 26.324 −20.573 1.00 44.92 ATOM 1611 O TRP A 911 −10.651 25.916 −21.384 1.00 45.96 ATOM 1612 CB TRP A 911 −12.481 28.625 −20.759 1.00 45.39 ATOM 1613 CG TRP A 911 −11.281 29.215 −21.435 1.00 49.15 ATOM 1614 CD1 TRP A 911 −11.238 29.822 −22.660 1.00 50.73 ATOM 1615 CD2 TRP A 911 −9.940 29.249 −20.924 1.00 50.38 ATOM 1616 NE1 TRP A 911 −9.954 30.237 −22.942 1.00 49.91 ATOM 1617 CE2 TRP A 911 −9.138 29.897 −21.892 1.00 51.44 ATOM 1618 CE3 TRP A 911 −9.339 28.794 −19.742 1.00 49.30 ATOM 1619 CZ2 TRP A 911 −7.763 30.101 −21.712 1.00 48.85 ATOM 1620 CZ3 TRP A 911 −7.973 28.997 −19.565 1.00 49.14 ATOM 1621 CH2 TRP A 911 −7.203 29.646 −20.548 1.00 48.84 ATOM 1622 N GLU A 912 −11.388 26.066 −19.268 1.00 44.35 ATOM 1623 CA GLU A 912 −10.277 25.273 −18.755 1.00 45.12 ATOM 1624 C GLU A 912 −10.299 23.922 −19.468 1.00 46.73 ATOM 1625 O GLU A 912 −9.254 23.400 −19.879 1.00 46.06 ATOM 1626 CB GLU A 912 −10.404 25.030 −17.247 1.00 44.17 ATOM 1627 CG GLU A 912 −10.530 26.265 −16.378 1.00 45.56 ATOM 1628 CD GLU A 912 −10.733 25.919 −14.899 1.00 47.51 ATOM 1629 OE1 GLU A 912 −9.766 25.474 −14.243 1.00 48.20 ATOM 1630 OE2 GLU A 912 −11.866 26.080 −14.389 1.00 46.43 ATOM 1631 N LEU A 913 −11.502 23.371 −19.622 1.00 46.87 ATOM 1632 CA LEU A 913 −11.691 22.072 −20.270 1.00 45.49 ATOM 1633 C LEU A 913 −11.261 22.067 −21.724 1.00 46.82 ATOM 1634 O LEU A 913 −10.522 21.179 −22.150 1.00 48.03 ATOM 1635 CB LEU A 913 −13.153 21.643 −20.170 1.00 43.18 ATOM 1636 CG LEU A 913 −13.750 21.713 −18.764 1.00 43.01 ATOM 1637 CD1 LEU A 913 −15.174 21.210 −18.804 1.00 43.13 ATOM 1638 CD2 LEU A 913 −12.916 20.880 −17.790 1.00 40.71 ATOM 1639 N MET A 914 −11.726 23.052 −22.487 1.00 48.63 ATOM 1640 CA MET A 914 −11.374 23.148 −23.903 1.00 50.01 ATOM 1641 C MET A 914 −9.874 23.324 −24.112 1.00 50.22 ATOM 1642 O MET A 914 −9.363 23.007 −25.182 1.00 50.31 ATOM 1643 CB MET A 914 −12.108 24.309 −24.576 1.00 51.66 ATOM 1644 CG MET A 914 −13.611 24.142 −24.660 1.00 54.12 ATOM 1645 SD MET A 914 −14.103 22.502 −25.184 1.00 55.78 ATOM 1646 CE MET A 914 −15.162 22.056 −23.847 1.00 54.82 ATOM 1647 N THR A 915 −9.171 23.846 −23.108 1.00 49.71 ATOM 1648 CA THR A 915 −7.727 24.013 −23.230 1.00 49.12 ATOM 1649 C THR A 915 −7.024 22.881 −22.487 1.00 50.59 ATOM 1650 O THR A 915 −5.851 22.985 −22.133 1.00 50.68 ATOM 1651 CB THR A 915 −7.240 25.361 −22.663 1.00 47.98 ATOM 1652 OG1 THR A 915 −7.532 25.426 −21.260 1.00 49.13 ATOM 1653 CG2 THR A 915 −7.912 26.526 −23.392 1.00 45.99 ATOM 1654 N PHE A 916 −7.756 21.797 −22.250 1.00 51.37 ATOM 1655 CA PHE A 916 −7.208 20.632 −21.571 1.00 51.95 ATOM 1656 C PHE A 916 −6.429 21.033 −20.317 1.00 53.29 ATOM 1657 O PHE A 916 −5.255 20.692 −20.160 1.00 54.44 ATOM 1658 CB PHE A 916 −6.299 19.861 −22.538 1.00 51.51 ATOM 1659 CG PHE A 916 −7.028 19.251 −23.718 1.00 50.02 ATOM 1660 CD1 PHE A 916 −7.835 18.124 −23.555 1.00 50.49 ATOM 1661 CD2 PHE A 916 −6.896 19.792 −24.988 1.00 47.97 ATOM 1662 CE1 PHE A 916 −8.493 17.548 −24.641 1.00 49.30 ATOM 1663 CE2 PHE A 916 −7.548 19.225 −26.073 1.00 49.17 ATOM 1664 CZ PHE A 916 −8.347 18.102 −25.902 1.00 49.74 ATOM 1665 N GLY A 917 −7.090 21.774 −19.433 1.00 54.12 ATOM 1666 CA GLY A 917 −6.455 22.207 −18.204 1.00 53.22 ATOM 1667 C GLY A 917 −5.687 23.516 −18.292 1.00 53.97 ATOM 1668 O GLY A 917 −4.769 23.745 −17.503 1.00 56.50 ATOM 1669 N GLY A 918 −6.046 24.385 −19.229 1.00 51.72 ATOM 1670 CA GLY A 918 −5.339 25.647 −19.336 1.00 52.43 ATOM 1671 C GLY A 918 −5.579 26.544 −18.135 1.00 54.51 ATOM 1672 O GLY A 918 −6.514 26.323 −17.366 1.00 55.43 ATOM 1673 N LYS A 919 −4.742 27.561 −17.964 1.00 55.17 ATOM 1674 CA LYS A 919 −4.902 28.472 −16.838 1.00 55.34 ATOM 1675 C LYS A 919 −5.396 29.852 −17.268 1.00 55.34 ATOM 1676 O LYS A 919 −4.765 30.528 −18.082 1.00 54.75 ATOM 1677 CB LYS A 919 −3.584 28.608 −16.082 1.00 57.86 ATOM 1678 CG LYS A 919 −3.045 27.296 −15.545 1.00 61.37 ATOM 1679 CD LYS A 919 −1.874 27.539 −14.608 1.00 65.00 ATOM 1680 CE LYS A 919 −2.319 28.318 −13.372 1.00 68.24 ATOM 1681 NZ LYS A 919 −1.174 28.718 −12.493 1.00 70.07 ATOM 1682 N PRO A 920 −6.539 30.287 −16.714 1.00 54.70 ATOM 1683 CA PRO A 920 −7.199 31.571 −16.977 1.00 54.08 ATOM 1684 C PRO A 920 −6.248 32.746 −16.833 1.00 53.70 ATOM 1685 O PRO A 920 −5.558 32.860 −15.828 1.00 54.60 ATOM 1686 CB PRO A 920 −8.292 31.617 −15.920 1.00 53.99 ATOM 1687 CG PRO A 920 −8.618 30.190 −15.718 1.00 56.24 ATOM 1688 CD PRO A 920 −7.269 29.535 −15.683 1.00 54.76 ATOM 1689 N TYR A 921 −6.232 33.624 −17.828 1.00 53.96 ATOM 1690 CA TYR A 921 −5.362 34.794 −17.810 1.00 56.43 ATOM 1691 C TYR A 921 −3.992 34.423 −17.242 1.00 59.51 ATOM 1692 O TYR A 921 −3.519 35.029 −16.276 1.00 59.77 ATOM 1693 CB TYR A 921 −5.996 35.904 −16.972 1.00 53.93 ATOM 1694 CG TYR A 921 −7.477 36.069 −17.217 1.00 50.28 ATOM 1695 CD1 TYR A 921 −8.406 35.456 −16.386 1.00 48.21 ATOM 1696 CD2 TYR A 921 −7.947 36.839 −18.281 1.00 47.29 ATOM 1697 CE1 TYR A 921 −9.760 35.604 −16.597 1.00 47.95 ATOM 1698 CE2 TYR A 921 −9.301 36.993 −18.503 1.00 46.64 ATOM 1699 CZ TYR A 921 −10.204 36.373 −17.654 1.00 48.17 ATOM 1700 OH TYR A 921 −11.552 36.534 −17.841 1.00 46.47 ATOM 1701 N ASP A 922 −3.369 33.424 −17.859 1.00 62.28 ATOM 1702 CA ASP A 922 −2.070 32.918 −17.437 1.00 65.68 ATOM 1703 C ASP A 922 −0.996 33.989 −17.291 1.00 67.52 ATOM 1704 O ASP A 922 −0.560 34.580 −18.281 1.00 68.07 ATOM 1705 CB ASP A 922 −1.573 31.869 −18.427 1.00 66.85 ATOM 1706 CG ASP A 922 −0.510 30.977 −17.830 1.00 69.00 ATOM 1707 OD1 ASP A 922 0.262 31.468 −16.972 1.00 68.93 ATOM 1708 OD2 ASP A 922 −0.445 29.790 −18.223 1.00 69.13 ATOM 1709 N GLY A 923 −0.564 34.221 −16.055 1.00 69.33 ATOM 1710 CA GLY A 923 0.468 35.212 −15.800 1.00 70.77 ATOM 1711 C GLY A 923 −0.022 36.553 −15.281 1.00 71.67 ATOM 1712 O GLY A 923 0.477 37.054 −14.270 1.00 72.97 ATOM 1713 N ILE A 924 −0.995 37.135 −15.973 1.00 71.05 ATOM 1714 CA ILE A 924 −1.548 38.428 −15.592 1.00 70.63 ATOM 1715 C ILE A 924 −1.781 38.545 −14.082 1.00 70.88 ATOM 1716 O ILE A 924 −2.336 37.640 −13.457 1.00 71.74 ATOM 1717 CB ILE A 924 −2.868 38.690 −16.349 1.00 70.59 ATOM 1718 CG1 ILE A 924 −2.652 38.433 −17.848 1.00 70.80 ATOM 1719 CG2 ILE A 924 −3.328 40.127 −16.124 1.00 68.25 ATOM 1720 CD1 ILE A 924 −3.930 38.442 −18.696 1.00 72.84 ATOM 1721 N PRO A 925 −1.340 39.668 −13.480 1.00 70.93 ATOM 1722 CA PRO A 925 −1.446 40.010 −12.055 1.00 70.60 ATOM 1723 C PRO A 925 −2.884 40.065 −11.539 1.00 69.81 ATOM 1724 O PRO A 925 −3.655 40.937 −11.933 1.00 67.59 ATOM 1725 CB PRO A 925 −0.779 41.384 −11.980 1.00 71.26 ATOM 1726 CG PRO A 925 0.207 41.347 −13.091 1.00 70.82 ATOM 1727 CD PRO A 925 −0.599 40.721 −14.196 1.00 70.92 ATOM 1728 N THR A 926 −3.221 39.149 −10.638 1.00 69.20 ATOM 1729 CA THR A 926 −4.559 39.071 −10.061 1.00 70.01 ATOM 1730 C THR A 926 −5.184 40.429 −9.730 1.00 70.43 ATOM 1731 O THR A 926 −6.407 40.578 −9.735 1.00 69.78 ATOM 1732 CB THR A 926 −4.553 38.213 −8.770 1.00 70.42 ATOM 1733 OG1 THR A 926 −5.899 37.915 −8.390 1.00 71.23 ATOM 1734 CG2 THR A 926 −3.870 38.962 −7.623 1.00 71.38 ATOM 1735 N ALA A 927 −4.344 41.417 −9.441 1.00 71.00 ATOM 1736 CA ALA A 927 −4.830 42.746 −9.095 1.00 70.88 ATOM 1737 C ALA A 927 −5.223 43.542 −10.336 1.00 71.19 ATOM 1738 O ALA A 927 −5.820 44.615 −10.237 1.00 72.20 ATOM 1739 CB ALA A 927 −3.759 43.498 −8.305 1.00 69.23 ATOM 1740 N GLU A 928 −4.908 43.008 −11.507 1.00 71.41 ATOM 1741 CA GLU A 928 −5.209 43.709 −12.747 1.00 71.50 ATOM 1742 C GLU A 928 −6.429 43.196 −13.494 1.00 68.69 ATOM 1743 O GLU A 928 −6.968 43.892 −14.355 1.00 68.39 ATOM 1744 CB GLU A 928 −3.983 43.669 −13.659 1.00 73.75 ATOM 1745 CG GLU A 928 −2.754 44.252 −12.996 1.00 78.75 ATOM 1746 CD GLU A 928 −1.535 44.234 −13.891 1.00 82.92 ATOM 1747 OE1 GLU A 928 −0.439 44.579 −13.390 1.00 85.58 ATOM 1748 OE2 GLU A 928 −1.672 43.880 −15.087 1.00 83.54 ATOM 1749 N ILE A 929 −6.868 41.988 −13.167 1.00 65.54 ATOM 1750 CA ILE A 929 −8.027 41.414 −13.831 1.00 63.43 ATOM 1751 C ILE A 929 −9.198 42.407 −13.900 1.00 62.00 ATOM 1752 O ILE A 929 −9.742 42.666 −14.973 1.00 58.78 ATOM 1753 CB ILE A 929 −8.482 40.126 −13.119 1.00 61.81 ATOM 1754 CG1 ILE A 929 −7.336 39.111 −13.105 1.00 61.74 ATOM 1755 CG2 ILE A 929 −9.689 39.538 −13.822 1.00 62.66 ATOM 1756 CD1 ILE A 929 −6.847 38.691 −14.478 1.00 59.86 ATOM 1757 N PRO A 930 −9.584 42.991 −12.755 1.00 61.97 ATOM 1758 CA PRO A 930 −10.694 43.948 −12.732 1.00 62.93 ATOM 1759 C PRO A 930 −10.643 44.976 −13.856 1.00 64.06 ATOM 1760 O PRO A 930 −11.641 45.216 −14.538 1.00 62.58 ATOM 1761 CB PRO A 930 −10.560 44.593 −11.358 1.00 61.80 ATOM 1762 CG PRO A 930 −10.047 43.479 −10.536 1.00 61.59 ATOM 1763 CD PRO A 930 −8.984 42.865 −11.417 1.00 60.70 ATOM 1764 N ASP A 931 −9.476 45.580 −14.046 1.00 66.03 ATOM 1765 CA ASP A 931 −9.311 46.589 −15.081 1.00 68.58 ATOM 1766 C ASP A 931 −9.354 46.006 −16.482 1.00 67.95 ATOM 1767 O ASP A 931 −10.012 46.563 −17.360 1.00 67.90 ATOM 1768 CB ASP A 931 −8.007 47.353 −14.866 1.00 73.60 ATOM 1769 CG ASP A 931 −8.015 48.146 −13.572 1.00 78.41 ATOM 1770 OD1 ASP A 931 −8.154 47.523 −12.485 1.00 79.78 ATOM 1771 OD2 ASP A 931 −7.890 49.391 −13.645 1.00 80.42 ATOM 1772 N LEU A 932 −8.654 44.896 −16.698 1.00 67.05 ATOM 1773 CA LEU A 932 −8.660 44.252 −18.007 1.00 66.68 ATOM 1774 C LEU A 932 −10.110 44.019 −18.434 1.00 67.26 ATOM 1775 O LEU A 932 −10.551 44.492 −19.484 1.00 67.71 ATOM 1776 CB LEU A 932 −7.932 42.909 −17.946 1.00 66.91 ATOM 1777 CG LEU A 932 −6.415 42.931 −17.754 1.00 68.66 ATOM 1778 CD1 LEU A 932 −5.905 41.504 −17.553 1.00 67.81 ATOM 1779 CD2 LEU A 932 −5.753 43.581 −18.977 1.00 68.04 ATOM 1780 N LEU A 933 −10.849 43.297 −17.599 1.00 66.10 ATOM 1781 CA LEU A 933 −12.240 42.982 −17.874 1.00 65.55 ATOM 1782 C LEU A 933 −13.049 44.190 −18.319 1.00 65.37 ATOM 1783 O LEU A 933 −13.751 44.135 −19.331 1.00 65.79 ATOM 1784 CB LEU A 933 −12.878 42.355 −16.638 1.00 64.86 ATOM 1785 CG LEU A 933 −12.233 41.030 −16.223 1.00 65.13 ATOM 1786 CD1 LEU A 933 −12.696 40.652 −14.828 1.00 65.75 ATOM 1787 CD2 LEU A 933 −12.579 39.945 −17.229 1.00 63.48 ATOM 1788 N GLU A 934 −12.947 45.280 −17.567 1.00 65.40 ATOM 1789 CA GLU A 934 −13.687 46.497 −17.885 1.00 65.09 ATOM 1790 C GLU A 934 −13.162 47.174 −19.132 1.00 63.61 ATOM 1791 O GLU A 934 −13.890 47.907 −19.797 1.00 61.44 ATOM 1792 CB GLU A 934 −13.657 47.451 −16.693 1.00 65.83 ATOM 1793 CG GLU A 934 −14.514 46.926 −15.558 1.00 71.06 ATOM 1794 CD GLU A 934 −14.315 47.656 −14.251 1.00 73.66 ATOM 1795 OE1 GLU A 934 −13.217 47.534 −13.659 1.00 75.01 ATOM 1796 OE2 GLU A 934 −15.267 48.344 −13.815 1.00 75.23 ATOM 1797 N LYS A 935 −11.896 46.926 −19.446 1.00 63.09 ATOM 1798 CA LYS A 935 −11.305 47.492 −20.644 1.00 64.10 ATOM 1799 C LYS A 935 −11.907 46.696 −21.792 1.00 64.34 ATOM 1800 O LYS A 935 −12.094 47.221 −22.884 1.00 65.68 ATOM 1801 CB LYS A 935 −9.787 47.316 −20.642 1.00 66.02 ATOM 1802 CG LYS A 935 −9.036 48.128 −19.598 1.00 68.95 ATOM 1803 CD LYS A 935 −8.968 49.594 −19.972 1.00 72.74 ATOM 1804 CE LYS A 935 −7.957 50.327 −19.106 1.00 74.63 ATOM 1805 NZ LYS A 935 −7.835 51.751 −19.525 1.00 76.76 ATOM 1806 N GLY A 936 −12.204 45.422 −21.534 1.00 62.92 ATOM 1807 CA GLY A 936 −12.800 44.578 −22.552 1.00 61.68 ATOM 1808 C GLY A 936 −12.202 43.192 −22.683 1.00 61.72 ATOM 1809 O GLY A 936 −12.830 42.298 −23.250 1.00 61.81 ATOM 1810 N GLU A 937 −10.991 43.013 −22.164 1.00 60.83 ATOM 1811 CA GLU A 937 −10.276 41.734 −22.217 1.00 59.06 ATOM 1812 C GLU A 937 −11.148 40.509 −21.889 1.00 57.16 ATOM 1813 O GLU A 937 −12.066 40.588 −21.073 1.00 56.93 ATOM 1814 CB GLU A 937 −9.086 41.774 −21.245 1.00 59.84 ATOM 1815 CG GLU A 937 −8.222 40.530 −21.268 1.00 62.61 ATOM 1816 CD GLU A 937 −6.844 40.793 −21.823 1.00 64.42 ATOM 1817 OE1 GLU A 937 −6.690 41.760 −22.595 1.00 64.76 ATOM 1818 OE2 GLU A 937 −5.916 40.024 −21.495 1.00 66.97 ATOM 1819 N ARG A 938 −10.842 39.382 −22.528 1.00 54.12 ATOM 1820 CA ARG A 938 −11.561 38.127 −22.311 1.00 51.97 ATOM 1821 C ARG A 938 −10.653 36.961 −22.658 1.00 51.14 ATOM 1822 O ARG A 938 −9.759 37.104 −23.486 1.00 54.50 ATOM 1823 CB ARG A 938 −12.810 38.053 −23.190 1.00 50.05 ATOM 1824 CG ARG A 938 −13.914 38.970 −22.756 1.00 48.91 ATOM 1825 CD ARG A 938 −14.329 38.646 −21.338 1.00 49.76 ATOM 1826 NE ARG A 938 −14.723 39.860 −20.636 1.00 54.12 ATOM 1827 CZ ARG A 938 −15.817 40.555 −20.911 1.00 53.77 ATOM 1828 NH1 ARG A 938 −16.624 40.141 −21.874 1.00 60.00 ATOM 1829 NH2 ARG A 938 −16.104 41.654 −20.235 1.00 48.85 ATOM 1830 N LEU A 939 −10.876 35.810 −22.035 1.00 47.64 ATOM 1831 CA LEU A 939 −10.059 34.647 −22.338 1.00 47.01 ATOM 1832 C LEU A 939 −10.058 34.409 −23.854 1.00 46.67 ATOM 1833 O LEU A 939 −11.041 34.691 −24.539 1.00 45.61 ATOM 1834 CB LEU A 939 −10.591 33.422 −21.587 1.00 46.49 ATOM 1835 CG LEU A 939 −10.427 33.537 −20.065 1.00 45.25 ATOM 1836 CD1 LEU A 939 −11.279 32.505 −19.343 1.00 43.35 ATOM 1837 CD2 LEU A 939 −8.968 33.376 −19.716 1.00 42.97 ATOM 1838 N PRO A 940 −8.943 33.896 −24.397 1.00 46.22 ATOM 1839 CA PRO A 940 −8.749 33.604 −25.826 1.00 44.26 ATOM 1840 C PRO A 940 −9.532 32.402 −26.327 1.00 45.20 ATOM 1841 O PRO A 940 −9.911 31.533 −25.555 1.00 46.46 ATOM 1842 CB PRO A 940 −7.252 33.336 −25.936 1.00 42.34 ATOM 1843 CG PRO A 940 −6.672 33.871 −24.654 1.00 46.14 ATOM 1844 CD PRO A 940 −7.726 33.590 −23.637 1.00 43.98 ATOM 1845 N GLN A 941 −9.737 32.346 −27.637 1.00 46.70 ATOM 1846 CA GLN A 941 −10.448 31.242 −28.263 1.00 46.31 ATOM 1847 C GLN A 941 −9.558 30.012 −28.242 1.00 46.69 ATOM 1848 O GLN A 941 −8.479 30.009 −28.824 1.00 46.60 ATOM 1849 CB GLN A 941 −10.810 31.605 −29.704 1.00 45.70 ATOM 1850 CG GLN A 941 −11.506 30.500 −30.467 1.00 46.44 ATOM 1851 CD GLN A 941 −12.083 30.960 −31.808 1.00 48.60 ATOM 1852 OE1 GLN A 941 −12.721 30.178 −32.521 1.00 47.90 ATOM 1853 NE2 GLN A 941 −11.861 32.226 −32.154 1.00 50.29 ATOM 1854 N PRO A 942 −9.992 28.950 −27.553 1.00 48.40 ATOM 1855 CA PRO A 942 −9.184 27.728 −27.490 1.00 49.09 ATOM 1856 C PRO A 942 −8.955 27.174 −28.894 1.00 50.75 ATOM 1857 O PRO A 942 −9.822 27.268 −29.755 1.00 52.32 ATOM 1858 CB PRO A 942 −10.036 26.793 −26.635 1.00 47.59 ATOM 1859 CG PRO A 942 −10.810 27.745 −25.767 1.00 49.17 ATOM 1860 CD PRO A 942 −11.210 28.822 −26.739 1.00 46.31 ATOM 1861 N PRO A 943 −7.781 26.584 −29.141 1.00 52.29 ATOM 1862 CA PRO A 943 −7.452 26.017 −30.450 1.00 51.87 ATOM 1863 C PRO A 943 −8.535 25.089 −31.025 1.00 52.45 ATOM 1864 O PRO A 943 −9.006 25.300 −32.147 1.00 53.80 ATOM 1865 CB PRO A 943 −6.149 25.270 −30.175 1.00 53.02 ATOM 1866 CG PRO A 943 −5.511 26.097 −29.120 1.00 52.76 ATOM 1867 CD PRO A 943 −6.670 26.391 −28.195 1.00 53.36 ATOM 1868 N ILE A 944 −8.927 24.073 −30.256 1.00 50.16 ATOM 1869 CA ILE A 944 −9.928 23.100 −30.702 1.00 48.57 ATOM 1870 C ILE A 944 −11.349 23.635 −30.776 1.00 49.82 ATOM 1871 O ILE A 944 −12.259 22.953 −31.268 1.00 47.90 ATOM 1872 CB ILE A 944 −9.973 21.876 −29.778 1.00 47.78 ATOM 1873 CG1 ILE A 944 −10.608 22.255 −28.430 1.00 43.48 ATOM 1874 CG2 ILE A 944 −8.579 21.321 −29.607 1.00 46.76 ATOM 1875 CD1 ILE A 944 −10.784 21.080 −27.499 1.00 42.87 ATOM 1876 N CYS A 945 −11.542 24.847 −30.275 1.00 51.05 ATOM 1877 CA CYS A 945 −12.860 25.449 −30.270 1.00 51.69 ATOM 1878 C CYS A 945 −13.254 26.015 −31.604 1.00 52.55 ATOM 1879 O CYS A 945 −12.490 26.739 −32.240 1.00 55.03 ATOM 1880 CB CYS A 945 −12.951 26.557 −29.217 1.00 52.52 ATOM 1881 SG CYS A 945 −13.270 25.971 −27.546 1.00 52.50 ATOM 1882 N THR A 946 −14.465 25.666 −32.011 1.00 51.88 ATOM 1883 CA THR A 946 −15.059 26.138 −33.246 1.00 50.67 ATOM 1884 C THR A 946 −15.703 27.448 −32.793 1.00 49.33 ATOM 1885 O THR A 946 −16.054 27.571 −31.626 1.00 49.43 ATOM 1886 CB THR A 946 −16.126 25.127 −33.733 1.00 50.13 ATOM 1887 OG1 THR A 946 −16.468 25.404 −35.091 1.00 52.85 ATOM 1888 CG2 THR A 946 −17.376 25.205 −32.871 1.00 46.57 ATOM 1889 N ILE A 947 −15.849 28.424 −33.684 1.00 49.50 ATOM 1890 CA ILE A 947 −16.436 29.705 −33.289 1.00 48.83 ATOM 1891 C ILE A 947 −17.843 29.569 −32.718 1.00 49.26 ATOM 1892 O ILE A 947 −18.415 30.527 −32.195 1.00 52.14 ATOM 1893 CB ILE A 947 −16.481 30.714 −34.454 1.00 48.12 ATOM 1894 CG1 ILE A 947 −16.732 32.121 −33.888 1.00 49.16 ATOM 1895 CG2 ILE A 947 −17.570 30.321 −35.452 1.00 46.40 ATOM 1896 CD1 ILE A 947 −16.721 33.247 −34.909 1.00 50.09 ATOM 1897 N ASP A 948 −18.407 28.379 −32.819 1.00 48.28 ATOM 1898 CA ASP A 948 −19.734 28.137 −32.279 1.00 47.63 ATOM 1899 C ASP A 948 −19.621 27.996 −30.761 1.00 46.50 ATOM 1900 O ASP A 948 −20.413 28.583 −30.012 1.00 46.41 ATOM 1901 CB ASP A 948 −20.311 26.857 −32.888 1.00 49.31 ATOM 1902 CG ASP A 948 −20.568 26.988 −34.377 1.00 49.35 ATOM 1903 OD1 ASP A 948 −21.612 27.553 −34.737 1.00 52.88 ATOM 1904 OD2 ASP A 948 −19.729 26.543 −35.186 1.00 50.17 ATOM 1905 N VAL A 949 −18.626 27.226 −30.317 1.00 43.56 ATOM 1906 CA VAL A 949 −18.405 26.998 −28.896 1.00 43.65 ATOM 1907 C VAL A 949 −17.894 28.262 −28.222 1.00 43.64 ATOM 1908 O VAL A 949 −18.333 28.619 −27.127 1.00 44.08 ATOM 1909 CB VAL A 949 −17.381 25.858 −28.654 1.00 43.97 ATOM 1910 CG1 VAL A 949 −17.132 25.689 −27.158 1.00 41.83 ATOM 1911 CG2 VAL A 949 −17.895 24.551 −29.246 1.00 41.36 ATOM 1912 N TYR A 950 −16.965 28.939 −28.885 1.00 43.36 ATOM 1913 CA TYR A 950 −16.395 30.160 −28.343 1.00 42.30 ATOM 1914 C TYR A 950 −17.478 31.180 −28.036 1.00 41.41 ATOM 1915 O TYR A 950 −17.489 31.774 −26.961 1.00 40.32 ATOM 1916 CB TYR A 950 −15.386 30.760 −29.322 1.00 43.03 ATOM 1917 CG TYR A 950 −14.489 31.806 −28.686 1.00 45.66 ATOM 1918 CD1 TYR A 950 −13.837 31.549 −27.473 1.00 45.82 ATOM 1919 CD2 TYR A 950 −14.283 33.044 −29.290 1.00 46.41 ATOM 1920 CE1 TYR A 950 −13.004 32.496 −26.879 1.00 44.71 ATOM 1921 CE2 TYR A 950 −13.446 34.002 −28.701 1.00 47.81 ATOM 1922 CZ TYR A 950 −12.811 33.715 −27.498 1.00 46.62 ATOM 1923 OH TYR A 950 −11.967 34.638 −26.931 1.00 46.10 ATOM 1924 N MET A 951 −18.390 31.386 −28.978 1.00 41.91 ATOM 1925 CA MET A 951 −19.459 32.343 −28.761 1.00 43.90 ATOM 1926 C MET A 951 −20.267 31.988 −27.532 1.00 44.53 ATOM 1927 O MET A 951 −20.776 32.877 −26.849 1.00 47.60 ATOM 1928 CB MET A 951 −20.366 32.447 −29.989 1.00 47.27 ATOM 1929 CG MET A 951 −19.674 33.105 −31.166 1.00 53.88 ATOM 1930 SD MET A 951 −18.776 34.589 −30.618 1.00 62.31 ATOM 1931 CE MET A 951 −20.155 35.487 −29.841 1.00 55.74 ATOM 1932 N VAL A 952 −20.397 30.700 −27.232 1.00 42.77 ATOM 1933 CA VAL A 952 −21.131 30.334 −26.031 1.00 42.94 ATOM 1934 C VAL A 952 −20.352 30.869 −24.819 1.00 44.09 ATOM 1935 O VAL A 952 −20.928 31.493 −23.923 1.00 44.56 ATOM 1936 CB VAL A 952 −21.341 28.795 −25.924 1.00 42.99 ATOM 1937 CG1 VAL A 952 −21.891 28.430 −24.551 1.00 39.35 ATOM 1938 CG2 VAL A 952 −22.332 28.339 −26.999 1.00 39.89 ATOM 1939 N MET A 953 −19.039 30.654 −24.807 1.00 44.23 ATOM 1940 CA MET A 953 −18.202 31.142 −23.711 1.00 45.49 ATOM 1941 C MET A 953 −18.231 32.670 −23.603 1.00 45.43 ATOM 1942 O MET A 953 −18.393 33.225 −22.510 1.00 45.00 ATOM 1943 CB MET A 953 −16.759 30.683 −23.900 1.00 44.82 ATOM 1944 CG MET A 953 −16.587 29.199 −23.816 1.00 48.13 ATOM 1945 SD MET A 953 −14.944 28.724 −24.267 1.00 52.76 ATOM 1946 CE MET A 953 −15.146 26.965 −24.437 1.00 52.38 ATOM 1947 N VAL A 954 −18.081 33.353 −24.734 1.00 42.69 ATOM 1948 CA VAL A 954 −18.086 34.804 −24.705 1.00 42.88 ATOM 1949 C VAL A 954 −19.408 35.363 −24.175 1.00 43.39 ATOM 1950 O VAL A 954 −19.402 36.290 −23.381 1.00 44.32 ATOM 1951 CB VAL A 954 −17.792 35.394 −26.090 1.00 42.98 ATOM 1952 CG1 VAL A 954 −17.863 36.890 −26.020 1.00 44.13 ATOM 1953 CG2 VAL A 954 −16.403 34.961 −26.565 1.00 43.05 ATOM 1954 N LYS A 955 −20.545 34.812 −24.589 1.00 43.09 ATOM 1955 CA LYS A 955 −21.814 35.327 −24.070 1.00 44.12 ATOM 1956 C LYS A 955 −21.844 35.189 −22.552 1.00 43.87 ATOM 1957 O LYS A 955 −22.417 36.024 −21.855 1.00 44.04 ATOM 1958 CB LYS A 955 −23.012 34.573 −24.656 1.00 45.68 ATOM 1959 CG LYS A 955 −23.304 34.831 −26.123 1.00 46.27 ATOM 1960 CD LYS A 955 −24.430 33.924 −26.563 1.00 46.94 ATOM 1961 CE LYS A 955 −24.660 33.965 −28.048 1.00 50.31 ATOM 1962 NZ LYS A 955 −25.433 32.759 −28.442 1.00 51.04 ATOM 1963 N CYS A 956 −21.238 34.123 −22.042 1.00 43.06 ATOM 1964 CA CYS A 956 −21.199 33.896 −20.602 1.00 43.04 ATOM 1965 C CYS A 956 −20.505 35.042 −19.861 1.00 44.88 ATOM 1966 O CYS A 956 −20.712 35.235 −18.652 1.00 42.74 ATOM 1967 CB CYS A 956 −20.453 32.606 −20.296 1.00 40.76 ATOM 1968 SG CYS A 956 −21.406 31.114 −20.517 1.00 40.75 ATOM 1969 N TRP A 957 −19.684 35.796 −20.593 1.00 46.16 ATOM 1970 CA TRP A 957 −18.929 36.888 −20.006 1.00 47.28 ATOM 1971 C TRP A 957 −19.409 38.283 −20.373 1.00 49.59 ATOM 1972 O TRP A 957 −18.629 39.231 −20.342 1.00 50.87 ATOM 1973 CB TRP A 957 −17.442 36.749 −20.365 1.00 44.94 ATOM 1974 CG TRP A 957 −16.881 35.389 −20.062 1.00 41.87 ATOM 1975 CD1 TRP A 957 −17.113 34.636 −18.949 1.00 40.97 ATOM 1976 CD2 TRP A 957 −15.987 34.628 −20.880 1.00 40.66 ATOM 1977 NE1 TRP A 957 −16.423 33.450 −19.022 1.00 41.10 ATOM 1978 CE2 TRP A 957 −15.720 33.419 −20.196 1.00 39.58 ATOM 1979 CE3 TRP A 957 −15.383 34.850 −22.125 1.00 39.57 ATOM 1980 CZ2 TRP A 957 −14.877 32.435 −20.712 1.00 39.64 ATOM 1981 CZ3 TRP A 957 −14.545 33.871 −22.639 1.00 40.43 ATOM 1982 CH2 TRP A 957 −14.298 32.676 −21.930 1.00 40.43 ATOM 1983 N MET A 958 −20.682 38.425 −20.720 1.00 50.92 ATOM 1984 CA MET A 958 −21.186 39.752 −21.048 1.00 52.62 ATOM 1985 C MET A 958 −21.165 40.609 −19.789 1.00 50.99 ATOM 1986 O MET A 958 −21.272 40.098 −18.676 1.00 49.32 ATOM 1987 CB MET A 958 −22.609 39.682 −21.598 1.00 54.02 ATOM 1988 CG MET A 958 −22.708 38.991 −22.941 1.00 57.72 ATOM 1989 SD MET A 958 −21.589 39.707 −24.136 1.00 61.72 ATOM 1990 CE MET A 958 −22.626 41.096 −24.754 1.00 62.55 ATOM 1991 N ILE A 959 −21.009 41.913 −19.968 1.00 51.63 ATOM 1992 CA ILE A 959 −20.979 42.819 −18.829 1.00 53.09 ATOM 1993 C ILE A 959 −22.342 42.742 −18.161 1.00 52.72 ATOM 1994 O ILE A 959 −22.461 42.808 −16.944 1.00 52.77 ATOM 1995 CB ILE A 959 −20.740 44.273 −19.267 1.00 53.98 ATOM 1996 CG1 ILE A 959 −19.387 44.387 −19.981 1.00 57.72 ATOM 1997 CG2 ILE A 959 −20.785 45.191 −18.050 1.00 53.54 ATOM 1998 CD1 ILE A 959 −19.163 45.733 −20.703 1.00 60.53 ATOM 1999 N ASP A 960 −23.374 42.584 −18.977 1.00 53.04 ATOM 2000 CA ASP A 960 −24.733 42.505 −18.472 1.00 54.30 ATOM 2001 C ASP A 960 −25.075 41.102 −17.961 1.00 53.33 ATOM 2002 O ASP A 960 −25.337 40.191 −18.739 1.00 50.47 ATOM 2003 CB ASP A 960 −25.706 42.903 −19.575 1.00 57.50 ATOM 2004 CG ASP A 960 −26.971 43.511 −19.035 1.00 59.92 ATOM 2005 OD1 ASP A 960 −27.626 42.880 −18.177 1.00 63.64 ATOM 2006 OD2 ASP A 960 −27.312 44.626 −19.476 1.00 62.47 ATOM 2007 N ALA A 961 −25.077 40.942 −16.646 1.00 53.51 ATOM 2008 CA ALA A 961 −25.384 39.659 −16.033 1.00 54.51 ATOM 2009 C ALA A 961 −26.650 39.046 −16.637 1.00 55.26 ATOM 2010 O ALA A 961 −26.690 37.856 −16.956 1.00 53.76 ATOM 2011 CB ALA A 961 −25.549 39.839 −14.528 1.00 52.04 ATOM 2012 N ASP A 962 −27.677 39.870 −16.804 1.00 56.69 ATOM 2013 CA ASP A 962 −28.942 39.405 −17.360 1.00 58.69 ATOM 2014 C ASP A 962 −28.948 38.994 −18.830 1.00 57.34 ATOM 2015 O ASP A 962 −29.803 38.211 −19.241 1.00 57.60 ATOM 2016 CB ASP A 962 −30.043 40.439 −17.118 1.00 61.14 ATOM 2017 CG ASP A 962 −30.633 40.339 −15.724 1.00 64.05 ATOM 2018 OD1 ASP A 962 −30.863 39.199 −15.259 1.00 62.71 ATOM 2019 OD2 ASP A 962 −30.876 41.396 −15.103 1.00 68.35 ATOM 2020 N SER A 963 −28.022 39.509 −19.631 1.00 56.01 ATOM 2021 CA SER A 963 −27.996 39.111 −21.031 1.00 54.55 ATOM 2022 C SER A 963 −27.117 37.870 −21.249 1.00 53.95 ATOM 2023 O SER A 963 −26.940 37.415 −22.378 1.00 55.77 ATOM 2024 CB SER A 963 −27.537 40.275 −21.925 1.00 55.92 ATOM 2025 OG SER A 963 −26.176 40.600 −21.734 1.00 55.38 ATOM 2026 N ARG A 964 −26.565 37.323 −20.170 1.00 51.26 ATOM 2027 CA ARG A 964 −25.746 36.115 −20.272 1.00 50.44 ATOM 2028 C ARG A 964 −26.711 34.942 −20.410 1.00 50.43 ATOM 2029 O ARG A 964 −27.820 34.970 −19.874 1.00 50.63 ATOM 2030 CB ARG A 964 −24.899 35.900 −19.010 1.00 47.22 ATOM 2031 CG ARG A 964 −23.902 36.994 −18.724 1.00 45.09 ATOM 2032 CD ARG A 964 −23.324 36.875 −17.329 1.00 42.47 ATOM 2033 NE ARG A 964 −22.590 38.085 −16.981 1.00 44.27 ATOM 2034 CZ ARG A 964 −22.156 38.392 −15.761 1.00 43.66 ATOM 2035 NH1 ARG A 964 −22.368 37.577 −14.736 1.00 38.19 ATOM 2036 NH2 ARG A 964 −21.527 39.543 −15.567 1.00 43.56 ATOM 2037 N PRO A 965 −26.303 33.891 −21.126 1.00 50.03 ATOM 2038 CA PRO A 965 −27.230 32.762 −21.256 1.00 50.55 ATOM 2039 C PRO A 965 −27.593 32.164 −19.890 1.00 50.02 ATOM 2040 O PRO A 965 −26.851 32.318 −18.920 1.00 50.28 ATOM 2041 CB PRO A 965 −26.460 31.786 −22.146 1.00 49.94 ATOM 2042 CG PRO A 965 −25.011 32.123 −21.855 1.00 51.67 ATOM 2043 CD PRO A 965 −25.011 33.617 −21.780 1.00 49.61 ATOM 2044 N LYS A 966 −28.748 31.515 −19.804 1.00 48.80 ATOM 2045 CA LYS A 966 −29.153 30.889 −18.554 1.00 48.28 ATOM 2046 C LYS A 966 −28.753 29.418 −18.572 1.00 47.56 ATOM 2047 O LYS A 966 −28.629 28.808 −19.642 1.00 45.03 ATOM 2048 CB LYS A 966 −30.654 31.021 −18.343 1.00 49.99 ATOM 2049 CG LYS A 966 −31.096 32.436 −18.067 1.00 55.88 ATOM 2050 CD LYS A 966 −32.242 32.462 −17.073 1.00 60.89 ATOM 2051 CE LYS A 966 −32.579 33.893 −16.660 1.00 64.65 ATOM 2052 NZ LYS A 966 −33.599 33.951 −15.563 1.00 65.07 ATOM 2053 N PHE A 967 −28.546 28.842 −17.392 1.00 45.93 ATOM 2054 CA PHE A 967 −28.138 27.449 −17.327 1.00 46.66 ATOM 2055 C PHE A 967 −29.005 26.499 −18.135 1.00 47.20 ATOM 2056 O PHE A 967 −28.518 25.470 −18.579 1.00 49.36 ATOM 2057 CB PHE A 967 −28.029 26.988 −15.875 1.00 46.03 ATOM 2058 CG PHE A 967 −26.767 27.437 −15.213 1.00 45.56 ATOM 2059 CD1 PHE A 967 −26.792 28.392 −14.199 1.00 45.88 ATOM 2060 CD2 PHE A 967 −25.535 26.971 −15.669 1.00 44.49 ATOM 2061 CE1 PHE A 967 −25.599 28.886 −13.650 1.00 47.81 ATOM 2062 CE2 PHE A 967 −24.340 27.455 −15.131 1.00 46.71 ATOM 2063 CZ PHE A 967 −24.368 28.416 −14.119 1.00 45.70 ATOM 2064 N ALA A 968 −30.275 26.846 −18.340 1.00 47.85 ATOM 2065 CA ALA A 968 −31.183 26.014 −19.136 1.00 48.27 ATOM 2066 C ALA A 968 −30.746 25.988 −20.615 1.00 49.39 ATOM 2067 O ALA A 968 −30.753 24.943 −21.264 1.00 49.53 ATOM 2068 CB ALA A 968 −32.620 26.542 −19.028 1.00 45.49 ATOM 2069 N GLU A 969 −30.358 27.142 −21.144 1.00 49.32 ATOM 2070 CA GLU A 969 −29.939 27.226 −22.533 1.00 48.74 ATOM 2071 C GLU A 969 −28.574 26.587 −22.760 1.00 48.05 ATOM 2072 O GLU A 969 −28.325 25.986 −23.812 1.00 47.73 ATOM 2073 CB GLU A 969 −29.863 28.682 −22.976 1.00 51.47 ATOM 2074 CG GLU A 969 −31.120 29.492 −22.779 1.00 55.25 ATOM 2075 CD GLU A 969 −30.928 30.929 −23.246 1.00 60.64 ATOM 2076 OE1 GLU A 969 −30.233 31.703 −22.539 1.00 58.91 ATOM 2077 OE2 GLU A 969 −31.454 31.274 −24.335 1.00 63.69 ATOM 2078 N LEU A 970 −27.681 26.739 −21.784 1.00 44.93 ATOM 2079 CA LEU A 970 −26.343 26.186 −21.918 1.00 42.24 ATOM 2080 C LEU A 970 −26.430 24.686 −22.019 1.00 41.43 ATOM 2081 O LEU A 970 −25.822 24.081 −22.901 1.00 40.90 ATOM 2082 CB LEU A 970 −25.450 26.611 −20.741 1.00 40.56 ATOM 2083 CG LEU A 970 −25.011 28.089 −20.768 1.00 37.75 ATOM 2084 CD1 LEU A 970 −24.376 28.470 −19.459 1.00 37.42 ATOM 2085 CD2 LEU A 970 −24.058 28.329 −21.906 1.00 32.61 ATOM 2086 N ALA A 971 −27.207 24.079 −21.134 1.00 41.36 ATOM 2087 CA ALA A 971 −27.350 22.634 −21.175 1.00 42.61 ATOM 2088 C ALA A 971 −27.934 22.243 −22.518 1.00 44.03 ATOM 2089 O ALA A 971 −27.470 21.309 −23.162 1.00 44.82 ATOM 2090 CB ALA A 971 −28.252 22.168 −20.074 1.00 42.94 ATOM 2091 N ALA A 972 −28.948 22.980 −22.941 1.00 43.93 ATOM 2092 CA ALA A 972 −29.600 22.705 −24.200 1.00 46.31 ATOM 2093 C ALA A 972 −28.675 22.874 −25.411 1.00 49.37 ATOM 2094 O ALA A 972 −28.638 22.013 −26.300 1.00 51.33 ATOM 2095 CB ALA A 972 −30.825 23.601 −24.342 1.00 43.28 ATOM 2096 N GLU A 973 −27.934 23.976 −25.454 1.00 50.72 ATOM 2097 CA GLU A 973 −27.045 24.243 −26.580 1.00 52.77 ATOM 2098 C GLU A 973 −25.930 23.205 −26.699 1.00 51.88 ATOM 2099 O GLU A 973 −25.721 22.643 −27.768 1.00 52.95 ATOM 2100 CB GLU A 973 −26.463 25.662 −26.450 1.00 57.46 ATOM 2101 CG GLU A 973 −25.475 26.119 −27.540 1.00 62.52 ATOM 2102 CD GLU A 973 −26.081 26.196 −28.944 1.00 67.05 ATOM 2103 OE1 GLU A 973 −27.304 26.435 −29.067 1.00 69.19 ATOM 2104 OE2 GLU A 973 −25.323 26.032 −29.930 1.00 68.06 ATOM 2105 N PHE A 974 −25.219 22.935 −25.609 1.00 49.75 ATOM 2106 CA PHE A 974 −24.134 21.965 −25.679 1.00 48.22 ATOM 2107 C PHE A 974 −24.698 20.605 −25.979 1.00 47.87 ATOM 2108 O PHE A 974 −24.088 19.806 −26.678 1.00 47.01 ATOM 2109 CB PHE A 974 −23.345 21.938 −24.374 1.00 46.42 ATOM 2110 CG PHE A 974 −22.362 23.053 −24.258 1.00 47.75 ATOM 2111 CD1 PHE A 974 −21.276 23.129 −25.128 1.00 48.10 ATOM 2112 CD2 PHE A 974 −22.547 24.071 −23.327 1.00 47.47 ATOM 2113 CE1 PHE A 974 −20.390 24.204 −25.077 1.00 46.79 ATOM 2114 CE2 PHE A 974 −21.673 25.148 −23.270 1.00 47.11 ATOM 2115 CZ PHE A 974 −20.588 25.215 −24.150 1.00 47.33 ATOM 2116 N SER A 975 −25.886 20.360 −25.446 1.00 47.80 ATOM 2117 CA SER A 975 −26.581 19.102 −25.644 1.00 47.24 ATOM 2118 C SER A 975 −26.704 18.813 −27.136 1.00 47.38 ATOM 2119 O SER A 975 −26.389 17.708 −27.588 1.00 47.22 ATOM 2120 CB SER A 975 −27.976 19.182 −25.022 1.00 48.16 ATOM 2121 OG SER A 975 −28.591 17.914 −24.947 1.00 49.36 ATOM 2122 N ARG A 976 −27.158 19.796 −27.910 1.00 45.99 ATOM 2123 CA ARG A 976 −27.301 19.558 −29.335 1.00 46.51 ATOM 2124 C ARG A 976 −25.925 19.475 −30.004 1.00 46.75 ATOM 2125 O ARG A 976 −25.779 18.840 −31.042 1.00 47.59 ATOM 2126 CB ARG A 976 −28.189 20.633 −29.988 1.00 44.73 ATOM 2127 CG ARG A 976 −27.436 21.795 −30.545 1.00 50.21 ATOM 2128 CD ARG A 976 −28.301 22.825 −31.270 1.00 51.39 ATOM 2129 NE ARG A 976 −27.435 23.946 −31.634 1.00 53.87 ATOM 2130 CZ ARG A 976 −26.509 23.885 −32.587 1.00 54.84 ATOM 2131 NH1 ARG A 976 −25.740 24.936 −32.849 1.00 56.13 ATOM 2132 NH2 ARG A 976 −26.383 22.784 −33.313 1.00 52.91 ATOM 2133 N MET A 977 −24.909 20.090 −29.406 1.00 48.59 ATOM 2134 CA MET A 977 −23.562 20.036 −29.979 1.00 50.45 ATOM 2135 C MET A 977 −22.996 18.635 −29.790 1.00 51.16 ATOM 2136 O MET A 977 −22.230 18.140 −30.620 1.00 51.33 ATOM 2137 CB MET A 977 −22.637 21.080 −29.324 1.00 51.44 ATOM 2138 CG MET A 977 −22.833 22.507 −29.861 1.00 54.98 ATOM 2139 SD MET A 977 −22.111 23.823 −28.853 1.00 58.42 ATOM 2140 CE MET A 977 −20.982 24.513 −29.911 1.00 56.62 ATOM 2141 N ALA A 978 −23.399 17.990 −28.703 1.00 51.59 ATOM 2142 CA ALA A 978 −22.938 16.646 −28.395 1.00 52.55 ATOM 2143 C ALA A 978 −23.492 15.596 −29.363 1.00 53.68 ATOM 2144 O ALA A 978 −22.947 14.501 −29.477 1.00 54.76 ATOM 2145 CB ALA A 978 −23.312 16.292 −26.959 1.00 50.13 ATOM 2146 N ARG A 979 −24.573 15.922 −30.058 1.00 55.30 ATOM 2147 CA ARG A 979 −25.156 14.983 −31.006 1.00 58.64 ATOM 2148 C ARG A 979 −24.312 14.943 −32.279 1.00 59.72 ATOM 2149 O ARG A 979 −24.554 14.127 −33.166 1.00 60.30 ATOM 2150 CB ARG A 979 −26.586 15.397 −31.370 1.00 60.38 ATOM 2151 CG ARG A 979 −27.545 15.474 −30.195 1.00 65.31 ATOM 2152 CD ARG A 979 −28.864 16.123 −30.604 1.00 67.03 ATOM 2153 NE ARG A 979 −29.575 16.664 −29.448 1.00 68.78 ATOM 2154 CZ ARG A 979 −30.539 17.581 −29.516 1.00 70.15 ATOM 2155 NH1 ARG A 979 −30.922 18.067 −30.694 1.00 70.75 ATOM 2156 NH2 ARG A 979 −31.107 18.027 −28.398 1.00 70.11 ATOM 2157 N ASP A 980 −23.325 15.827 −32.365 1.00 59.38 ATOM 2158 CA ASP A 980 −22.464 15.903 −33.541 1.00 59.02 ATOM 2159 C ASP A 980 −21.190 16.645 −33.122 1.00 57.66 ATOM 2160 O ASP A 980 −20.858 17.709 −33.649 1.00 56.21 ATOM 2161 CB ASP A 980 −23.215 16.654 −34.649 1.00 60.77 ATOM 2162 CG ASP A 980 −22.502 16.607 −35.990 1.00 62.49 ATOM 2163 OD1 ASP A 980 −21.643 15.717 −36.183 1.00 64.46 ATOM 2164 OD2 ASP A 980 −22.821 17.456 −36.858 1.00 61.55 ATOM 2165 N PRO A 981 −20.453 16.066 −32.162 1.00 56.22 ATOM 2166 CA PRO A 981 −19.208 16.598 −31.598 1.00 55.44 ATOM 2167 C PRO A 981 −18.084 17.037 −32.535 1.00 53.93 ATOM 2168 O PRO A 981 −17.492 18.090 −32.323 1.00 53.34 ATOM 2169 CB PRO A 981 −18.772 15.496 −30.629 1.00 55.07 ATOM 2170 CG PRO A 981 −19.345 14.262 −31.229 1.00 54.89 ATOM 2171 CD PRO A 981 −20.718 14.715 −31.637 1.00 55.91 ATOM 2172 N GLN A 982 −17.773 16.245 −33.556 1.00 54.01 ATOM 2173 CA GLN A 982 −16.698 16.617 −34.476 1.00 53.13 ATOM 2174 C GLN A 982 −17.043 17.886 −35.253 1.00 50.44 ATOM 2175 O GLN A 982 −16.188 18.476 −35.897 1.00 48.82 ATOM 2176 CB GLN A 982 −16.377 15.470 −35.445 1.00 55.75 ATOM 2177 CG GLN A 982 −15.535 14.333 −34.851 1.00 59.04 ATOM 2178 CD GLN A 982 −16.299 13.465 −33.854 1.00 63.65 ATOM 2179 OE1 GLN A 982 −17.524 13.576 −33.721 1.00 65.05 ATOM 2180 NE2 GLN A 982 −15.578 12.605 −33.140 1.00 65.14 ATOM 2181 N ARG A 983 −18.296 18.311 −35.179 1.00 49.29 ATOM 2182 CA ARG A 983 −18.716 19.528 −35.861 1.00 49.03 ATOM 2183 C ARG A 983 −18.482 20.771 −35.012 1.00 47.62 ATOM 2184 O ARG A 983 −18.549 21.890 −35.514 1.00 48.25 ATOM 2185 CB ARG A 983 −20.196 19.479 −36.200 1.00 50.98 ATOM 2186 CG ARG A 983 −20.683 20.768 −36.834 1.00 53.68 ATOM 2187 CD ARG A 983 −22.171 20.801 −36.932 1.00 55.23 ATOM 2188 NE ARG A 983 −22.623 21.823 −37.864 1.00 57.30 ATOM 2189 CZ ARG A 983 −23.903 22.094 −38.081 1.00 58.03 ATOM 2190 NH1 ARG A 983 −24.838 21.416 −37.424 1.00 59.36 ATOM 2191 NH2 ARG A 983 −24.247 23.028 −38.954 1.00 57.21 ATOM 2192 N TYR A 984 −18.217 20.585 −33.727 1.00 46.14 ATOM 2193 CA TYR A 984 −18.005 21.728 −32.860 1.00 46.62 ATOM 2194 C TYR A 984 −16.629 21.830 −32.178 1.00 45.34 ATOM 2195 O TYR A 984 −16.165 22.923 −31.866 1.00 44.15 ATOM 2196 CB TYR A 984 −19.162 21.797 −31.855 1.00 45.73 ATOM 2197 CG TYR A 984 −20.483 22.095 −32.545 1.00 47.52 ATOM 2198 CD1 TYR A 984 −21.367 21.075 −32.892 1.00 49.29 ATOM 2199 CD2 TYR A 984 −20.816 23.401 −32.920 1.00 47.84 ATOM 2200 CE1 TYR A 984 −22.553 21.352 −33.598 1.00 48.94 ATOM 2201 CE2 TYR A 984 −21.987 23.683 −33.622 1.00 47.24 ATOM 2202 CZ TYR A 984 −22.847 22.658 −33.957 1.00 48.48 ATOM 2203 OH TYR A 984 −23.996 22.944 −34.655 1.00 50.81 ATOM 2204 N LEU A 985 −15.976 20.698 −31.957 1.00 44.95 ATOM 2205 CA LEU A 985 −14.648 20.689 −31.353 1.00 45.72 ATOM 2206 C LEU A 985 −13.746 19.932 −32.320 1.00 47.79 ATOM 2207 O LEU A 985 −14.094 18.836 −32.770 1.00 47.32 ATOM 2208 CB LEU A 985 −14.672 19.980 −29.997 1.00 44.68 ATOM 2209 CG LEU A 985 −15.410 20.665 −28.849 1.00 44.43 ATOM 2210 CD1 LEU A 985 −15.243 19.853 −27.574 1.00 43.38 ATOM 2211 CD2 LEU A 985 −14.860 22.079 −28.660 1.00 44.96 ATOM 2212 N VAL A 986 −12.596 20.510 −32.647 1.00 48.85 ATOM 2213 CA VAL A 986 −11.679 19.871 −33.582 1.00 49.84 ATOM 2214 C VAL A 986 −10.398 19.397 −32.911 1.00 51.24 ATOM 2215 O VAL A 986 −9.426 20.136 −32.805 1.00 51.87 ATOM 2216 CB VAL A 986 −11.312 20.828 −34.716 1.00 51.14 ATOM 2217 CG1 VAL A 986 −10.392 20.130 −35.709 1.00 50.04 ATOM 2218 CG2 VAL A 986 −12.573 21.325 −35.394 1.00 49.84 ATOM 2219 N ILE A 987 −10.406 18.146 −32.473 1.00 53.09 ATOM 2220 CA ILE A 987 −9.267 17.541 −31.797 1.00 52.98 ATOM 2221 C ILE A 987 −8.535 16.595 −32.736 1.00 55.59 ATOM 2222 O ILE A 987 −9.155 15.754 −33.392 1.00 53.71 ATOM 2223 CB ILE A 987 −9.735 16.727 −30.591 1.00 50.88 ATOM 2224 CG1 ILE A 987 −10.571 17.611 −29.665 1.00 52.22 ATOM 2225 CG2 ILE A 987 −8.549 16.124 −29.884 1.00 49.91 ATOM 2226 CD1 ILE A 987 −11.307 16.840 −28.586 1.00 49.45 ATOM 2227 N GLN A 988 −7.214 16.723 −32.792 1.00 59.02 ATOM 2228 CA GLN A 988 −6.418 15.860 −33.645 1.00 61.68 ATOM 2229 C GLN A 988 −6.654 14.424 −33.178 1.00 64.13 ATOM 2230 O GLN A 988 −6.577 14.127 −31.980 1.00 62.70 ATOM 2231 CB GLN A 988 −4.946 16.236 −33.528 1.00 63.64 ATOM 2232 CG GLN A 988 −4.134 15.850 −34.745 1.00 67.15 ATOM 2233 CD GLN A 988 −2.726 16.407 −34.726 1.00 67.61 ATOM 2234 OE1 GLN A 988 −1.961 16.193 −35.659 1.00 71.31 ATOM 2235 NE2 GLN A 988 −2.378 17.124 −33.665 1.00 70.34 ATOM 2236 N GLY A 989 −6.947 13.542 −34.131 1.00 66.36 ATOM 2237 CA GLY A 989 −7.240 12.156 −33.809 1.00 68.95 ATOM 2238 C GLY A 989 −8.751 12.071 −33.788 1.00 71.82 ATOM 2239 O GLY A 989 −9.386 12.067 −34.840 1.00 73.55 ATOM 2240 N ASP A 990 −9.317 12.011 −32.586 1.00 74.05 ATOM 2241 CA ASP A 990 −10.766 11.986 −32.362 1.00 75.83 ATOM 2242 C ASP A 990 −11.591 11.562 −33.583 1.00 77.60 ATOM 2243 O ASP A 990 −12.564 12.219 −33.951 1.00 77.72 ATOM 2244 CB ASP A 990 −11.194 13.387 −31.870 1.00 73.28 ATOM 2245 CG ASP A 990 −12.647 13.457 −31.412 1.00 70.03 ATOM 2246 OD1 ASP A 990 −13.121 12.530 −30.715 1.00 70.19 ATOM 2247 OD2 ASP A 990 −13.308 14.466 −31.732 1.00 65.64 ATOM 2248 N ALA A 991 −11.208 10.456 −34.208 1.00 80.41 ATOM 2249 CA ALA A 991 −11.936 9.974 −35.374 1.00 83.98 ATOM 2250 C ALA A 991 −12.676 8.672 −35.059 1.00 86.60 ATOM 2251 O ALA A 991 −13.837 8.503 −35.441 1.00 87.41 ATOM 2252 CB ALA A 991 −10.972 9.771 −36.550 1.00 82.75 ATOM 2253 N ALA A 992 −12.005 7.767 −34.347 1.00 88.48 ATOM 2254 CA ALA A 992 −12.582 6.471 −33.992 1.00 90.40 ATOM 2255 C ALA A 992 −12.798 6.298 −32.492 1.00 91.49 ATOM 2256 O ALA A 992 −13.875 5.784 −32.113 1.00 91.08 ATOM 2257 CB ALA A 992 −11.694 5.350 −34.516 1.00 90.58 ATOM 2258 OXT ALA A 992 −11.879 6.655 −31.721 1.00 92.46 ATOM 2259 N ALA B 694 −21.367 6.079 −64.456 1.00 78.72 ATOM 2260 CA ALA B 694 −22.190 6.371 −63.252 1.00 78.66 ATOM 2261 C ALA B 694 −21.358 7.182 −62.263 1.00 78.89 ATOM 2262 O ALA B 694 −20.424 7.882 −62.653 1.00 79.39 ATOM 2263 CB ALA B 694 −22.652 5.062 −62.614 1.00 77.87 ATOM 2264 N ALA B 695 −21.703 7.085 −60.984 1.00 78.95 ATOM 2265 CA ALA B 695 −20.990 7.791 −59.923 1.00 78.98 ATOM 2266 C ALA B 695 −20.828 6.832 −58.742 1.00 79.45 ATOM 2267 O ALA B 695 −21.816 6.296 −58.240 1.00 80.20 ATOM 2268 CB ALA B 695 −21.775 9.030 −59.498 1.00 77.61 ATOM 2269 N ALA B 696 −19.588 6.618 −58.305 1.00 79.38 ATOM 2270 CA ALA B 696 −19.298 5.702 −57.200 1.00 79.53 ATOM 2271 C ALA B 696 −20.251 5.840 −56.006 1.00 80.35 ATOM 2272 O ALA B 696 −20.595 6.950 −55.604 1.00 80.03 ATOM 2273 CB ALA B 696 −17.849 5.883 −56.742 1.00 77.04 ATOM 2274 N PRO B 697 −20.699 4.701 −55.435 1.00 81.52 ATOM 2275 CA PRO B 697 −21.611 4.620 −54.284 1.00 81.54 ATOM 2276 C PRO B 697 −21.046 5.326 −53.053 1.00 82.10 ATOM 2277 O PRO B 697 −19.916 5.067 −52.635 1.00 82.80 ATOM 2278 CB PRO B 697 −21.752 3.118 −54.058 1.00 81.54 ATOM 2279 CG PRO B 697 −21.616 2.564 −55.434 1.00 82.60 ATOM 2280 CD PRO B 697 −20.452 3.355 −55.987 1.00 82.37 ATOM 2281 N LEU B 698 −21.845 6.207 −52.467 1.00 81.85 ATOM 2282 CA LEU B 698 −21.421 6.969 −51.303 1.00 80.76 ATOM 2283 C LEU B 698 −21.365 6.109 −50.051 1.00 79.77 ATOM 2284 O LEU B 698 −21.874 4.994 −50.048 1.00 80.40 ATOM 2285 CB LEU B 698 −22.383 8.136 −51.093 1.00 80.50 ATOM 2286 CG LEU B 698 −22.038 9.096 −49.959 1.00 80.61 ATOM 2287 CD1 LEU B 698 −20.711 9.781 −50.243 1.00 80.34 ATOM 2288 CD2 LEU B 698 −23.150 10.118 −49.823 1.00 80.62 ATOM 2289 N THR B 699 −20.732 6.641 −49.006 1.00 79.28 ATOM 2290 CA THR B 699 −20.585 5.992 −47.692 1.00 79.67 ATOM 2291 C THR B 699 −19.385 6.573 −46.938 1.00 78.91 ATOM 2292 O THR B 699 −18.317 5.969 −46.894 1.00 79.37 ATOM 2293 CB THR B 699 −20.408 4.444 −47.792 1.00 80.11 ATOM 2294 OG1 THR B 699 −19.202 4.135 −48.503 1.00 80.37 ATOM 2295 CG2 THR B 699 −21.616 3.801 −48.481 1.00 78.91 ATOM 2296 N PRO B 700 −19.555 7.757 −46.324 1.00 78.42 ATOM 2297 CA PRO B 700 −18.508 8.454 −45.566 1.00 78.09 ATOM 2298 C PRO B 700 −17.960 7.713 −44.354 1.00 77.41 ATOM 2299 O PRO B 700 −18.560 6.759 −43.863 1.00 77.46 ATOM 2300 CB PRO B 700 −19.182 9.764 −45.176 1.00 77.99 ATOM 2301 CG PRO B 700 −20.601 9.355 −45.002 1.00 78.57 ATOM 2302 CD PRO B 700 −20.833 8.482 −46.218 1.00 78.31 ATOM 2303 N SER B 701 −16.811 8.175 −43.876 1.00 76.96 ATOM 2304 CA SER B 701 −16.150 7.577 −42.725 1.00 76.79 ATOM 2305 C SER B 701 −15.878 8.645 −41.676 1.00 76.45 ATOM 2306 O SER B 701 −16.079 9.838 −41.920 1.00 76.52 ATOM 2307 CB SER B 701 −14.824 6.944 −43.154 1.00 77.52 ATOM 2308 OG SER B 701 −13.944 7.924 −43.690 1.00 77.51 ATOM 2309 N GLY B 702 −15.418 8.221 −40.507 1.00 75.81 ATOM 2310 CA GLY B 702 −15.123 9.188 −39.466 1.00 75.42 ATOM 2311 C GLY B 702 −14.011 10.118 −39.912 1.00 73.55 ATOM 2312 O GLY B 702 −14.195 11.334 −40.015 1.00 73.83 ATOM 2313 N THR B 703 −12.858 9.521 −40.194 1.00 71.08 ATOM 2314 CA THR B 703 −11.662 10.227 −40.629 1.00 68.76 ATOM 2315 C THR B 703 −11.903 11.547 −41.346 1.00 66.14 ATOM 2316 O THR B 703 −12.657 11.616 −42.309 1.00 66.70 ATOM 2317 CB THR B 703 −10.826 9.341 −41.553 1.00 70.67 ATOM 2318 OG1 THR B 703 −10.649 8.051 −40.948 1.00 72.31 ATOM 2319 CG2 THR B 703 −9.466 9.982 −41.809 1.00 71.40 ATOM 2320 N ALA B 704 −11.244 12.596 −40.871 1.00 62.68 ATOM 2321 CA ALA B 704 −11.370 13.915 −41.469 1.00 59.07 ATOM 2322 C ALA B 704 −10.277 14.034 −42.529 1.00 57.68 ATOM 2323 O ALA B 704 −9.333 13.236 −42.556 1.00 56.92 ATOM 2324 CB ALA B 704 −11.210 14.992 −40.403 1.00 56.44 ATOM 2325 N PRO B 705 −10.387 15.030 −43.418 1.00 54.82 ATOM 2326 CA PRO B 705 −9.393 15.215 −44.473 1.00 53.14 ATOM 2327 C PRO B 705 −8.001 15.562 −43.982 1.00 52.08 ATOM 2328 O PRO B 705 −7.835 16.297 −43.019 1.00 52.38 ATOM 2329 CB PRO B 705 −9.995 16.328 −45.317 1.00 53.47 ATOM 2330 CG PRO B 705 −10.713 17.142 −44.308 1.00 53.49 ATOM 2331 CD PRO B 705 −11.394 16.102 −43.457 1.00 53.49 ATOM 2332 N ASN B 706 −7.005 15.018 −44.668 1.00 50.16 ATOM 2333 CA ASN B 706 −5.614 15.255 −44.352 1.00 47.68 ATOM 2334 C ASN B 706 −5.141 16.419 −45.220 1.00 48.60 ATOM 2335 O ASN B 706 −4.817 16.235 −46.394 1.00 47.17 ATOM 2336 CB ASN B 706 −4.798 14.007 −44.679 1.00 46.68 ATOM 2337 CG ASN B 706 −3.336 14.152 −44.307 1.00 47.50 ATOM 2338 OD1 ASN B 706 −2.843 15.264 −44.085 1.00 46.16 ATOM 2339 ND2 ASN B 706 −2.624 13.025 −44.252 1.00 47.14 ATOM 2340 N GLN B 707 −5.089 17.616 −44.654 1.00 48.45 ATOM 2341 CA GLN B 707 −4.663 18.753 −45.448 1.00 50.34 ATOM 2342 C GLN B 707 −3.195 19.132 −45.296 1.00 49.32 ATOM 2343 O GLN B 707 −2.820 20.282 −45.508 1.00 48.81 ATOM 2344 CB GLN B 707 −5.565 19.961 −45.172 1.00 51.33 ATOM 2345 CG GLN B 707 −7.017 19.707 −45.534 1.00 54.04 ATOM 2346 CD GLN B 707 −7.890 20.942 −45.390 1.00 57.85 ATOM 2347 OE1 GLN B 707 −7.874 21.834 −46.244 1.00 59.23 ATOM 2348 NE2 GLN B 707 −8.651 21.007 −44.296 1.00 57.51 ATOM 2349 N ALA B 708 −2.361 18.160 −44.944 1.00 49.01 ATOM 2350 CA ALA B 708 −0.930 18.416 −44.814 1.00 49.28 ATOM 2351 C ALA B 708 −0.402 18.939 −46.153 1.00 50.28 ATOM 2352 O ALA B 708 −0.927 18.609 −47.216 1.00 50.22 ATOM 2353 CB ALA B 708 −0.201 17.134 −44.434 1.00 46.73 ATOM 2354 N GLN B 709 0.635 19.761 −46.102 1.00 52.30 ATOM 2355 CA GLN B 709 1.209 20.305 −47.320 1.00 53.30 ATOM 2356 C GLN B 709 2.521 19.639 −47.662 1.00 54.63 ATOM 2357 O GLN B 709 3.328 19.342 −46.788 1.00 55.25 ATOM 2358 CB GLN B 709 1.438 21.807 −47.173 1.00 53.77 ATOM 2359 CG GLN B 709 0.187 22.623 −47.359 1.00 56.18 ATOM 2360 CD GLN B 709 −0.326 22.555 −48.777 1.00 58.18 ATOM 2361 OE1 GLN B 709 −1.494 22.832 −49.037 1.00 59.37 ATOM 2362 NE2 GLN B 709 0.553 22.197 −49.710 1.00 59.96 ATOM 2363 N LEU B 710 2.734 19.394 −48.943 1.00 56.61 ATOM 2364 CA LEU B 710 3.984 18.793 −49.368 1.00 59.18 ATOM 2365 C LEU B 710 4.565 19.616 −50.508 1.00 59.54 ATOM 2366 O LEU B 710 4.077 19.563 −51.634 1.00 60.05 ATOM 2367 CB LEU B 710 3.788 17.341 −49.826 1.00 58.84 ATOM 2368 CG LEU B 710 5.144 16.673 −50.079 1.00 58.85 ATOM 2369 CD1 LEU B 710 5.941 16.662 −48.780 1.00 56.82 ATOM 2370 CD2 LEU B 710 4.960 15.272 −50.610 1.00 59.31 ATOM 2371 N ARG B 711 5.602 20.385 −50.201 1.00 59.61 ATOM 2372 CA ARG B 711 6.249 21.218 −51.199 1.00 59.44 ATOM 2373 C ARG B 711 7.209 20.387 −52.020 1.00 57.96 ATOM 2374 O ARG B 711 8.038 19.665 −51.487 1.00 56.87 ATOM 2375 CB ARG B 711 7.026 22.352 −50.528 1.00 62.07 ATOM 2376 CG ARG B 711 6.173 23.468 −49.947 1.00 66.77 ATOM 2377 CD ARG B 711 6.166 24.664 −50.880 1.00 70.76 ATOM 2378 NE ARG B 711 5.529 25.830 −50.275 1.00 73.86 ATOM 2379 CZ ARG B 711 5.482 27.030 −50.849 1.00 73.77 ATOM 2380 NH1 ARG B 711 6.038 27.213 −52.039 1.00 71.33 ATOM 2381 NH2 ARG B 711 4.872 28.041 −50.241 1.00 74.12 ATOM 2382 N ILE B 712 7.073 20.472 −53.331 1.00 58.48 ATOM 2383 CA ILE B 712 7.968 19.765 −54.221 1.00 59.27 ATOM 2384 C ILE B 712 8.952 20.858 −54.638 1.00 60.66 ATOM 2385 O ILE B 712 8.601 21.793 −55.355 1.00 60.01 ATOM 2386 CB ILE B 712 7.177 19.162 −55.390 1.00 58.30 ATOM 2387 CG1 ILE B 712 6.266 18.066 −54.826 1.00 57.96 ATOM 2388 CG2 ILE B 712 8.117 18.601 −56.448 1.00 56.69 ATOM 2389 CD1 ILE B 712 5.405 17.380 −55.840 1.00 61.91 ATOM 2390 N LEU B 713 10.178 20.744 −54.139 1.00 60.97 ATOM 2391 CA LEU B 713 11.201 21.748 −54.374 1.00 61.57 ATOM 2392 C LEU B 713 12.091 21.583 −55.583 1.00 62.89 ATOM 2393 O LEU B 713 12.517 20.476 −55.921 1.00 62.63 ATOM 2394 CB LEU B 713 12.093 21.864 −53.141 1.00 60.62 ATOM 2395 CG LEU B 713 11.375 21.861 −51.796 1.00 60.72 ATOM 2396 CD1 LEU B 713 12.345 22.362 −50.739 1.00 60.07 ATOM 2397 CD2 LEU B 713 10.134 22.743 −51.848 1.00 58.84 ATOM 2398 N ALA B 714 12.388 22.713 −56.216 1.00 63.60 ATOM 2399 CA ALA B 714 13.257 22.724 −57.373 1.00 64.47 ATOM 2400 C ALA B 714 14.663 22.544 −56.828 1.00 65.36 ATOM 2401 O ALA B 714 15.049 23.194 −55.857 1.00 64.64 ATOM 2402 CB ALA B 714 13.136 24.052 −58.115 1.00 65.35 ATOM 2403 N GLU B 715 15.409 21.642 −57.451 1.00 66.38 ATOM 2404 CA GLU B 715 16.786 21.337 −57.075 1.00 68.71 ATOM 2405 C GLU B 715 17.570 22.608 −56.764 1.00 69.58 ATOM 2406 O GLU B 715 18.489 22.606 −55.945 1.00 70.53 ATOM 2407 CB GLU B 715 17.451 20.590 −58.233 1.00 71.46 ATOM 2408 CG GLU B 715 18.838 20.031 −57.972 1.00 75.03 ATOM 2409 CD GLU B 715 19.366 19.255 −59.174 1.00 78.03 ATOM 2410 OE1 GLU B 715 20.444 18.627 −59.064 1.00 81.21 ATOM 2411 OE2 GLU B 715 18.699 19.275 −60.234 1.00 78.12 ATOM 2412 N THR B 716 17.178 23.692 −57.422 1.00 69.78 ATOM 2413 CA THR B 716 17.825 24.987 −57.283 1.00 69.47 ATOM 2414 C THR B 716 17.451 25.789 −56.041 1.00 69.52 ATOM 2415 O THR B 716 18.240 26.611 −55.573 1.00 70.64 ATOM 2416 CB THR B 716 17.536 25.866 −58.513 1.00 70.06 ATOM 2417 OG1 THR B 716 18.171 27.138 −58.351 1.00 71.27 ATOM 2418 CG2 THR B 716 16.036 26.076 −58.678 1.00 69.60 ATOM 2419 N GLU B 717 16.253 25.577 −55.511 1.00 68.00 ATOM 2420 CA GLU B 717 15.845 26.321 −54.330 1.00 66.43 ATOM 2421 C GLU B 717 16.699 25.898 −53.135 1.00 66.27 ATOM 2422 O GLU B 717 16.735 26.588 −52.117 1.00 65.77 ATOM 2423 CB GLU B 717 14.363 26.072 −54.032 1.00 67.50 ATOM 2424 CG GLU B 717 13.430 26.254 −55.234 1.00 67.97 ATOM 2425 CD GLU B 717 11.971 25.930 −54.911 1.00 68.95 ATOM 2426 OE1 GLU B 717 11.314 25.253 −55.736 1.00 69.80 ATOM 2427 OE2 GLU B 717 11.479 26.355 −53.843 1.00 67.07 ATOM 2428 N LEU B 718 17.409 24.778 −53.277 1.00 66.24 ATOM 2429 CA LEU B 718 18.240 24.241 −52.197 1.00 67.00 ATOM 2430 C LEU B 718 19.741 24.416 −52.344 1.00 68.38 ATOM 2431 O LEU B 718 20.308 24.173 −53.410 1.00 68.22 ATOM 2432 CB LEU B 718 17.961 22.746 −51.989 1.00 64.67 ATOM 2433 CG LEU B 718 16.592 22.299 −51.473 1.00 64.09 ATOM 2434 CD1 LEU B 718 16.642 20.805 −51.218 1.00 64.50 ATOM 2435 CD2 LEU B 718 16.221 23.038 −50.196 1.00 61.97 ATOM 2436 N ALA B 719 20.376 24.807 −51.240 1.00 69.63 ATOM 2437 CA ALA B 719 21.820 25.008 −51.188 1.00 70.57 ATOM 2438 C ALA B 719 22.409 24.242 −50.006 1.00 71.59 ATOM 2439 O ALA B 719 21.972 24.404 −48.859 1.00 71.07 ATOM 2440 CB ALA B 719 22.152 26.499 −51.062 1.00 69.58 ATOM 2441 N ARG B 720 23.399 23.404 −50.303 1.00 72.39 ATOM 2442 CA ARG B 720 24.083 22.601 −49.296 1.00 73.45 ATOM 2443 C ARG B 720 25.143 23.436 −48.577 1.00 74.60 ATOM 2444 O ARG B 720 25.385 24.593 −48.911 1.00 75.29 ATOM 2445 CB ARG B 720 24.786 21.414 −49.952 1.00 73.03 ATOM 2446 CG ARG B 720 23.902 20.485 −50.756 1.00 74.45 ATOM 2447 CD ARG B 720 23.856 19.106 −50.118 1.00 75.59 ATOM 2448 NE ARG B 720 23.875 18.018 −51.097 1.00 76.81 ATOM 2449 CZ ARG B 720 22.976 17.855 −52.063 1.00 76.86 ATOM 2450 NH1 ARG B 720 21.972 18.714 −52.198 1.00 76.25 ATOM 2451 NH2 ARG B 720 23.074 16.818 −52.886 1.00 77.66 ATOM 2452 N VAL B 721 25.774 22.831 −47.583 1.00 75.37 ATOM 2453 CA VAL B 721 26.835 23.472 −46.824 1.00 75.73 ATOM 2454 C VAL B 721 27.804 22.356 −46.447 1.00 76.50 ATOM 2455 O VAL B 721 28.600 21.912 −47.275 1.00 76.71 ATOM 2456 CB VAL B 721 26.297 24.148 −45.550 1.00 76.20 ATOM 2457 CG1 VAL B 721 27.451 24.684 −44.722 1.00 76.08 ATOM 2458 CG2 VAL B 721 25.358 25.282 −45.925 1.00 75.75 ATOM 2459 N ALA B 722 27.722 21.889 −45.208 1.00 77.05 ATOM 2460 CA ALA B 722 28.584 20.809 −44.751 1.00 76.34 ATOM 2461 C ALA B 722 27.735 19.558 −44.559 1.00 75.78 ATOM 2462 O ALA B 722 26.537 19.548 −44.868 1.00 75.60 ATOM 2463 CB ALA B 722 29.262 21.196 −43.433 1.00 76.05 ATOM 2464 N VAL B 723 28.373 18.507 −44.053 1.00 74.68 ATOM 2465 CA VAL B 723 27.714 17.239 −43.777 1.00 71.94 ATOM 2466 C VAL B 723 27.423 17.159 −42.283 1.00 71.54 ATOM 2467 O VAL B 723 28.310 17.399 −41.461 1.00 71.55 ATOM 2468 CB VAL B 723 28.611 16.058 −44.160 1.00 71.07 ATOM 2469 CG1 VAL B 723 28.020 14.767 −43.629 1.00 70.27 ATOM 2470 CG2 VAL B 723 28.764 15.998 −45.672 1.00 71.21 ATOM 2471 N LEU B 724 26.182 16.836 −41.931 1.00 69.67 ATOM 2472 CA LEU B 724 25.806 16.721 −40.529 1.00 66.81 ATOM 2473 C LEU B 724 26.058 15.300 −40.057 1.00 66.43 ATOM 2474 O LEU B 724 26.094 15.032 −38.859 1.00 68.21 ATOM 2475 CB LEU B 724 24.334 17.080 −40.347 1.00 64.61 ATOM 2476 CG LEU B 724 23.992 18.555 −40.555 1.00 64.25 ATOM 2477 CD1 LEU B 724 22.493 18.740 −40.600 1.00 62.81 ATOM 2478 CD2 LEU B 724 24.593 19.379 −39.431 1.00 63.59 ATOM 2479 N GLY B 725 26.248 14.403 −41.018 1.00 65.74 ATOM 2480 CA GLY B 725 26.484 13.004 −40.723 1.00 65.55 ATOM 2481 C GLY B 725 25.812 12.138 −41.777 1.00 67.20 ATOM 2482 O GLY B 725 24.919 12.602 −42.487 1.00 67.07 ATOM 2483 N SER B 726 26.241 10.884 −41.888 1.00 68.22 ATOM 2484 CA SER B 726 25.668 9.957 −42.860 1.00 69.48 ATOM 2485 C SER B 726 25.632 8.553 −42.275 1.00 70.10 ATOM 2486 O SER B 726 26.012 8.344 −41.126 1.00 71.12 ATOM 2487 CB SER B 726 26.504 9.935 −44.139 1.00 70.71 ATOM 2488 OG SER B 726 27.715 9.214 −43.947 1.00 71.56 ATOM 2489 N GLY B 727 25.186 7.593 −43.079 1.00 71.04 ATOM 2490 CA GLY B 727 25.109 6.217 −42.623 1.00 72.17 ATOM 2491 C GLY B 727 24.190 5.350 −43.469 1.00 72.74 ATOM 2492 O GLY B 727 23.941 5.645 −44.642 1.00 73.49 ATOM 2493 N ALA B 728 23.683 4.280 −42.865 1.00 72.58 ATOM 2494 CA ALA B 728 22.794 3.342 −43.539 1.00 72.96 ATOM 2495 C ALA B 728 21.657 4.049 −44.263 1.00 74.25 ATOM 2496 O ALA B 728 21.285 3.682 −45.381 1.00 73.50 ATOM 2497 CB ALA B 728 22.226 2.361 −42.527 1.00 71.89 ATOM 2498 N PHE B 729 21.110 5.071 −43.618 1.00 76.13 ATOM 2499 CA PHE B 729 20.003 5.825 −44.186 1.00 78.00 ATOM 2500 C PHE B 729 20.488 7.116 −44.823 1.00 78.39 ATOM 2501 O PHE B 729 20.531 8.153 −44.167 1.00 80.61 ATOM 2502 CB PHE B 729 18.980 6.125 −43.091 1.00 78.54 ATOM 2503 CG PHE B 729 18.734 4.958 −42.176 1.00 80.05 ATOM 2504 CD1 PHE B 729 19.552 4.741 −41.067 1.00 80.31 ATOM 2505 CD2 PHE B 729 17.731 4.029 −42.464 1.00 80.12 ATOM 2506 CE1 PHE B 729 19.379 3.613 −40.258 1.00 79.48 ATOM 2507 CE2 PHE B 729 17.551 2.902 −41.666 1.00 79.41 ATOM 2508 CZ PHE B 729 18.378 2.694 −40.561 1.00 80.03 ATOM 2509 N GLY B 730 20.867 7.040 −46.098 1.00 77.21 ATOM 2510 CA GLY B 730 21.343 8.209 −46.819 1.00 75.57 ATOM 2511 C GLY B 730 22.288 9.121 −46.055 1.00 74.55 ATOM 2512 O GLY B 730 22.876 8.721 −45.051 1.00 74.34 ATOM 2513 N THR B 731 22.447 10.349 −46.540 1.00 73.71 ATOM 2514 CA THR B 731 23.322 11.316 −45.887 1.00 72.89 ATOM 2515 C THR B 731 22.575 12.607 −45.597 1.00 72.69 ATOM 2516 O THR B 731 21.765 13.069 −46.406 1.00 72.79 ATOM 2517 CB THR B 731 24.547 11.650 −46.751 1.00 73.00 ATOM 2518 OG1 THR B 731 25.364 10.484 −46.894 1.00 72.99 ATOM 2519 CG2 THR B 731 25.367 12.753 −46.100 1.00 72.78 ATOM 2520 N VAL B 732 22.854 13.186 −44.434 1.00 72.09 ATOM 2521 CA VAL B 732 22.204 14.422 −44.025 1.00 71.72 ATOM 2522 C VAL B 732 23.109 15.616 −44.283 1.00 71.79 ATOM 2523 O VAL B 732 24.312 15.553 −44.053 1.00 73.24 ATOM 2524 CB VAL B 732 21.817 14.385 −42.525 1.00 71.31 ATOM 2525 CG1 VAL B 732 21.170 15.704 −42.124 1.00 70.14 ATOM 2526 CG2 VAL B 732 20.858 13.220 −42.256 1.00 69.55 ATOM 2527 N TYR B 733 22.517 16.703 −44.762 1.00 71.37 ATOM 2528 CA TYR B 733 23.256 17.915 −45.072 1.00 70.26 ATOM 2529 C TYR B 733 22.636 19.144 −44.437 1.00 70.40 ATOM 2530 O TYR B 733 21.423 19.328 −44.475 1.00 69.19 ATOM 2531 CB TYR B 733 23.280 18.136 −46.581 1.00 71.02 ATOM 2532 CG TYR B 733 24.205 17.228 −47.350 1.00 72.14 ATOM 2533 CD1 TYR B 733 25.552 17.550 −47.516 1.00 72.40 ATOM 2534 CD2 TYR B 733 23.733 16.051 −47.928 1.00 72.72 ATOM 2535 CE1 TYR B 733 26.403 16.722 −48.244 1.00 72.86 ATOM 2536 CE2 TYR B 733 24.573 15.215 −48.654 1.00 72.43 ATOM 2537 CZ TYR B 733 25.904 15.556 −48.807 1.00 72.95 ATOM 2538 OH TYR B 733 26.734 14.728 −49.519 1.00 73.75 ATOM 2539 N LYS B 734 23.468 19.988 −43.845 1.00 71.52 ATOM 2540 CA LYS B 734 22.971 21.235 −43.278 1.00 71.70 ATOM 2541 C LYS B 734 22.836 22.110 −44.526 1.00 70.70 ATOM 2542 O LYS B 734 23.636 21.981 −45.457 1.00 69.26 ATOM 2543 CB LYS B 734 24.000 21.843 −42.323 1.00 72.03 ATOM 2544 CG LYS B 734 23.619 23.219 −41.810 1.00 73.15 ATOM 2545 CD LYS B 734 24.811 23.927 −41.173 1.00 74.86 ATOM 2546 CE LYS B 734 24.469 25.371 −40.815 1.00 75.25 ATOM 2547 NZ LYS B 734 25.609 26.084 −40.177 1.00 75.36 ATOM 2548 N GLY B 735 21.836 22.983 −44.570 1.00 69.60 ATOM 2549 CA GLY B 735 21.694 23.804 −45.757 1.00 70.34 ATOM 2550 C GLY B 735 20.674 24.921 −45.717 1.00 70.22 ATOM 2551 O GLY B 735 20.003 25.146 −44.709 1.00 70.41 ATOM 2552 N ILE B 736 20.559 25.626 −46.835 1.00 70.46 ATOM 2553 CA ILE B 736 19.619 26.730 −46.932 1.00 71.88 ATOM 2554 C ILE B 736 18.619 26.490 −48.053 1.00 70.97 ATOM 2555 O ILE B 736 18.988 26.084 −49.158 1.00 70.48 ATOM 2556 CB ILE B 736 20.344 28.065 −47.216 1.00 73.37 ATOM 2557 CG1 ILE B 736 21.503 28.253 −46.232 1.00 75.08 ATOM 2558 CG2 ILE B 736 19.359 29.225 −47.099 1.00 72.22 ATOM 2559 CD1 ILE B 736 22.363 29.482 −46.523 1.00 77.81 ATOM 2560 N TRP B 737 17.349 26.734 −47.756 1.00 69.75 ATOM 2561 CA TRP B 737 16.301 26.571 −48.746 1.00 69.68 ATOM 2562 C TRP B 737 15.679 27.924 −49.044 1.00 71.04 ATOM 2563 O TRP B 737 15.167 28.593 −48.142 1.00 70.73 ATOM 2564 CB TRP B 737 15.219 25.612 −48.247 1.00 67.06 ATOM 2565 CG TRP B 737 13.973 25.642 −49.085 1.00 63.60 ATOM 2566 CD1 TRP B 737 13.900 25.681 −50.449 1.00 62.26 ATOM 2567 CD2 TRP B 737 12.623 25.615 −48.614 1.00 62.62 ATOM 2568 NE1 TRP B 737 12.589 25.683 −50.857 1.00 61.65 ATOM 2569 CE2 TRP B 737 11.783 25.641 −49.752 1.00 61.65 ATOM 2570 CE3 TRP B 737 12.041 25.567 −47.342 1.00 62.03 ATOM 2571 CZ2 TRP B 737 10.393 25.621 −49.658 1.00 61.01 ATOM 2572 CZ3 TRP B 737 10.657 25.545 −47.246 1.00 63.21 ATOM 2573 CH2 TRP B 737 9.847 25.573 −48.402 1.00 62.84 ATOM 2574 N VAL B 738 15.727 28.320 −50.313 1.00 71.93 ATOM 2575 CA VAL B 738 15.162 29.590 −50.738 1.00 72.89 ATOM 2576 C VAL B 738 13.895 29.317 −51.539 1.00 74.11 ATOM 2577 O VAL B 738 13.960 29.000 −52.722 1.00 74.51 ATOM 2578 CB VAL B 738 16.155 30.357 −51.614 1.00 73.24 ATOM 2579 CG1 VAL B 738 15.753 31.811 −51.677 1.00 72.41 ATOM 2580 CG2 VAL B 738 17.573 30.189 −51.067 1.00 71.96 ATOM 2581 N PRO B 739 12.723 29.441 −50.898 1.00 75.71 ATOM 2582 CA PRO B 739 11.408 29.212 −51.504 1.00 78.23 ATOM 2583 C PRO B 739 11.246 29.754 −52.922 1.00 80.64 ATOM 2584 O PRO B 739 11.912 30.716 −53.309 1.00 80.64 ATOM 2585 CB PRO B 739 10.462 29.882 −50.518 1.00 77.56 ATOM 2586 CG PRO B 739 11.135 29.618 −49.210 1.00 77.83 ATOM 2587 CD PRO B 739 12.574 29.957 −49.527 1.00 76.20 ATOM 2588 N ALA B 740 10.348 29.128 −53.682 1.00 83.02 ATOM 2589 CA ALA B 740 10.077 29.521 −55.062 1.00 84.99 ATOM 2590 C ALA B 740 9.540 30.948 −55.142 1.00 86.49 ATOM 2591 O ALA B 740 8.328 31.168 −55.063 1.00 87.30 ATOM 2592 CB ALA B 740 9.080 28.554 −55.695 1.00 84.35 ATOM 2593 N GLY B 741 10.449 31.912 −55.293 1.00 87.21 ATOM 2594 CA GLY B 741 10.048 33.306 −55.390 1.00 88.15 ATOM 2595 C GLY B 741 10.039 34.051 −54.069 1.00 88.91 ATOM 2596 O GLY B 741 9.134 34.841 −53.796 1.00 89.07 ATOM 2597 N GLU B 742 11.051 33.804 −53.245 1.00 89.01 ATOM 2598 CA GLU B 742 11.146 34.460 −51.949 1.00 89.25 ATOM 2599 C GLU B 742 12.605 34.733 −51.597 1.00 89.18 ATOM 2600 O GLU B 742 13.514 34.121 −52.163 1.00 87.36 ATOM 2601 CB GLU B 742 10.486 33.592 −50.874 1.00 89.33 ATOM 2602 CG GLU B 742 9.030 33.270 −51.166 1.00 89.86 ATOM 2603 CD GLU B 742 8.394 32.409 −50.096 1.00 91.41 ATOM 2604 OE1 GLU B 742 7.217 32.022 −50.259 1.00 92.46 ATOM 2605 OE2 GLU B 742 9.068 32.116 −49.089 1.00 91.98 ATOM 2606 N ALA B 743 12.818 35.659 −50.664 1.00 89.63 ATOM 2607 CA ALA B 743 14.163 36.037 −50.241 1.00 89.61 ATOM 2608 C ALA B 743 14.626 35.259 −49.016 1.00 89.33 ATOM 2609 O ALA B 743 15.813 34.951 −48.884 1.00 89.32 ATOM 2610 CB ALA B 743 14.219 37.538 −49.956 1.00 88.93 ATOM 2611 N VAL B 744 13.692 34.944 −48.122 1.00 88.36 ATOM 2612 CA VAL B 744 14.016 34.203 −46.902 1.00 86.73 ATOM 2613 C VAL B 744 14.987 33.060 −47.185 1.00 85.49 ATOM 2614 O VAL B 744 14.800 32.293 −48.129 1.00 86.20 ATOM 2615 CB VAL B 744 12.744 33.615 −46.239 1.00 86.40 ATOM 2616 CG1 VAL B 744 11.827 34.737 −45.777 1.00 86.46 ATOM 2617 CG2 VAL B 744 12.018 32.709 −47.217 1.00 86.17 ATOM 2618 N ALA B 745 16.033 32.959 −46.373 1.00 83.22 ATOM 2619 CA ALA B 745 17.020 31.901 −46.537 1.00 80.32 ATOM 2620 C ALA B 745 16.858 30.887 −45.402 1.00 78.54 ATOM 2621 O ALA B 745 17.722 30.780 −44.537 1.00 77.78 ATOM 2622 CB ALA B 745 18.426 32.497 −46.528 1.00 79.74 ATOM 2623 N ILE B 746 15.742 30.154 −45.415 1.00 76.18 ATOM 2624 CA ILE B 746 15.427 29.144 −44.394 1.00 73.00 ATOM 2625 C ILE B 746 16.506 28.085 −44.148 1.00 70.60 ATOM 2626 O ILE B 746 16.926 27.379 −45.068 1.00 70.94 ATOM 2627 CB ILE B 746 14.133 28.384 −44.740 1.00 73.31 ATOM 2628 CG1 ILE B 746 12.939 29.338 −44.735 1.00 74.65 ATOM 2629 CG2 ILE B 746 13.906 27.271 −43.733 1.00 73.54 ATOM 2630 CD1 ILE B 746 11.630 28.690 −45.169 1.00 74.90 ATOM 2631 N PRO B 747 16.963 27.959 −42.890 1.00 68.46 ATOM 2632 CA PRO B 747 17.991 26.973 −42.542 1.00 66.18 ATOM 2633 C PRO B 747 17.322 25.609 −42.442 1.00 63.94 ATOM 2634 O PRO B 747 16.327 25.441 −41.727 1.00 62.47 ATOM 2635 CB PRO B 747 18.499 27.475 −41.198 1.00 65.24 ATOM 2636 CG PRO B 747 17.258 28.014 −40.581 1.00 65.83 ATOM 2637 CD PRO B 747 16.625 28.788 −41.718 1.00 67.44 ATOM 2638 N VAL B 748 17.864 24.638 −43.162 1.00 61.19 ATOM 2639 CA VAL B 748 17.273 23.316 −43.161 1.00 60.40 ATOM 2640 C VAL B 748 18.273 22.179 −43.190 1.00 60.05 ATOM 2641 O VAL B 748 19.484 22.383 −43.273 1.00 59.27 ATOM 2642 CB VAL B 748 16.346 23.121 −44.382 1.00 60.82 ATOM 2643 CG1 VAL B 748 15.250 24.166 −44.384 1.00 60.94 ATOM 2644 CG2 VAL B 748 17.159 23.192 −45.662 1.00 58.19 ATOM 2645 N ALA B 749 17.726 20.973 −43.110 1.00 59.07 ATOM 2646 CA ALA B 749 18.503 19.757 −43.177 1.00 59.25 ATOM 2647 C ALA B 749 18.025 19.161 −44.489 1.00 60.46 ATOM 2648 O ALA B 749 16.899 19.422 −44.910 1.00 61.58 ATOM 2649 CB ALA B 749 18.159 18.837 −42.019 1.00 57.97 ATOM 2650 N ILE B 750 18.881 18.388 −45.144 1.00 60.55 ATOM 2651 CA ILE B 750 18.536 17.762 −46.407 1.00 59.69 ATOM 2652 C ILE B 750 19.113 16.364 −46.376 1.00 60.35 ATOM 2653 O ILE B 750 20.304 16.182 −46.120 1.00 59.91 ATOM 2654 CB ILE B 750 19.152 18.519 −47.593 1.00 60.90 ATOM 2655 CG1 ILE B 750 18.855 20.014 −47.470 1.00 61.45 ATOM 2656 CG2 ILE B 750 18.593 17.976 −48.898 1.00 61.29 ATOM 2657 CD1 ILE B 750 19.552 20.868 −48.512 1.00 62.03 ATOM 2658 N LYS B 751 18.272 15.373 −46.629 1.00 60.64 ATOM 2659 CA LYS B 751 18.736 14.003 −46.608 1.00 61.71 ATOM 2660 C LYS B 751 18.568 13.371 −47.970 1.00 64.10 ATOM 2661 O LYS B 751 17.569 13.593 −48.652 1.00 63.74 ATOM 2662 CB LYS B 751 17.962 13.216 −45.557 1.00 60.11 ATOM 2663 CG LYS B 751 18.422 11.788 −45.379 1.00 58.61 ATOM 2664 CD LYS B 751 17.930 11.241 −44.049 1.00 58.06 ATOM 2665 CE LYS B 751 18.424 9.840 −43.818 1.00 56.70 ATOM 2666 NZ LYS B 751 18.112 9.366 −42.448 1.00 57.25 ATOM 2667 N ILE B 752 19.562 12.590 −48.367 1.00 67.30 ATOM 2668 CA ILE B 752 19.532 11.909 −49.650 1.00 70.25 ATOM 2669 C ILE B 752 19.714 10.425 −49.393 1.00 71.94 ATOM 2670 O ILE B 752 20.740 10.013 −48.867 1.00 73.06 ATOM 2671 CB ILE B 752 20.666 12.407 −50.556 1.00 70.74 ATOM 2672 CG1 ILE B 752 20.578 13.930 −50.705 1.00 70.64 ATOM 2673 CG2 ILE B 752 20.578 11.721 −51.912 1.00 71.95 ATOM 2674 CD1 ILE B 752 21.674 14.538 −51.555 1.00 69.52 ATOM 2675 N ALA B 753 18.723 9.623 −49.760 1.00 74.71 ATOM 2676 CA ALA B 753 18.799 8.185 −49.536 1.00 78.36 ATOM 2677 C ALA B 753 19.570 7.481 −50.639 1.00 81.19 ATOM 2678 O ALA B 753 19.369 7.757 −51.821 1.00 81.29 ATOM 2679 CB ALA B 753 17.399 7.601 −49.423 1.00 77.47 ATOM 2680 N VAL B 754 20.453 6.570 −50.238 1.00 85.07 ATOM 2681 CA VAL B 754 21.281 5.798 −51.170 1.00 88.42 ATOM 2682 C VAL B 754 20.468 5.271 −52.358 1.00 90.41 ATOM 2683 O VAL B 754 19.817 4.229 −52.260 1.00 91.29 ATOM 2684 CB VAL B 754 21.940 4.581 −50.459 1.00 88.45 ATOM 2685 CG1 VAL B 754 23.015 3.969 −51.357 1.00 86.93 ATOM 2686 CG2 VAL B 754 22.519 5.009 −49.108 1.00 88.93 ATOM 2687 N ALA B 755 20.517 5.991 −53.477 1.00 91.96 ATOM 2688 CA ALA B 755 19.789 5.605 −54.684 1.00 93.14 ATOM 2689 CB ALA B 755 20.303 6.403 −55.878 1.00 92.70 ATOM 2690 C ALA B 755 19.890 4.104 −54.975 1.00 94.28 ATOM 2691 OT1 ALA B 755 18.831 3.482 −55.224 1.00 94.26 ATOM 2692 OT2 ALA B 755 21.023 3.569 −54.962 1.00 94.42 ATOM 2693 N ALA B 761 9.723 1.143 −56.947 1.00 87.14 ATOM 2694 CA ALA B 761 10.011 1.599 −55.557 1.00 87.01 ATOM 2695 C ALA B 761 9.596 3.053 −55.300 1.00 87.49 ATOM 2696 O ALA B 761 9.028 3.358 −54.254 1.00 88.29 ATOM 2697 CB ALA B 761 11.492 1.420 −55.252 1.00 86.17 ATOM 2698 N ASN B 762 9.879 3.946 −56.245 1.00 87.30 ATOM 2699 CA ASN B 762 9.532 5.358 −56.091 1.00 86.68 ATOM 2700 C ASN B 762 8.123 5.587 −55.563 1.00 85.76 ATOM 2701 O ASN B 762 7.796 6.676 −55.095 1.00 85.55 ATOM 2702 CB ASN B 762 9.711 6.095 −57.417 1.00 87.83 ATOM 2703 CG ASN B 762 11.145 6.515 −57.652 1.00 88.91 ATOM 2704 OD1 ASN B 762 12.065 5.696 −57.587 1.00 88.14 ATOM 2705 ND2 ASN B 762 11.347 7.800 −57.923 1.00 89.08 ATOM 2706 N VAL B 763 7.288 4.559 −55.645 1.00 84.95 ATOM 2707 CA VAL B 763 5.919 4.652 −55.152 1.00 83.59 ATOM 2708 C VAL B 763 5.981 4.500 −53.634 1.00 82.82 ATOM 2709 O VAL B 763 5.380 5.277 −52.891 1.00 82.67 ATOM 2710 CB VAL B 763 5.039 3.517 −55.713 1.00 83.22 ATOM 2711 CG1 VAL B 763 3.574 3.913 −55.639 1.00 83.32 ATOM 2712 CG2 VAL B 763 5.452 3.190 −57.134 1.00 83.28 ATOM 2713 N ALA B 764 6.723 3.485 −53.192 1.00 81.06 ATOM 2714 CA ALA B 764 6.899 3.188 −51.774 1.00 79.39 ATOM 2715 C ALA B 764 7.374 4.428 −51.024 1.00 77.74 ATOM 2716 O ALA B 764 7.068 4.616 −49.841 1.00 77.59 ATOM 2717 CB ALA B 764 7.911 2.048 −51.601 1.00 78.81 ATOM 2718 N PHE B 765 8.124 5.269 −51.727 1.00 75.13 ATOM 2719 CA PHE B 765 8.653 6.497 −51.156 1.00 72.04 ATOM 2720 C PHE B 765 7.617 7.621 −51.141 1.00 69.21 ATOM 2721 O PHE B 765 7.398 8.271 −50.120 1.00 67.19 ATOM 2722 CB PHE B 765 9.890 6.937 −51.939 1.00 72.95 ATOM 2723 CG PHE B 765 10.256 8.364 −51.716 1.00 74.51 ATOM 2724 CD1 PHE B 765 9.604 9.378 −52.416 1.00 76.66 ATOM 2725 CD2 PHE B 765 11.187 8.708 −50.749 1.00 74.99 ATOM 2726 CE1 PHE B 765 9.868 10.717 −52.152 1.00 76.83 ATOM 2727 CE2 PHE B 765 11.460 10.042 −50.474 1.00 76.87 ATOM 2728 CZ PHE B 765 10.797 11.053 −51.177 1.00 77.47 ATOM 2729 N MET B 766 6.989 7.858 −52.281 1.00 67.05 ATOM 2730 CA MET B 766 5.990 8.903 −52.362 1.00 66.91 ATOM 2731 C MET B 766 4.876 8.664 −51.351 1.00 66.11 ATOM 2732 O MET B 766 4.201 9.598 −50.924 1.00 66.81 ATOM 2733 CB MET B 766 5.412 8.975 −53.778 1.00 68.18 ATOM 2734 CG MET B 766 6.425 9.399 −54.826 1.00 68.28 ATOM 2735 SD MET B 766 7.326 10.874 −54.318 1.00 68.93 ATOM 2736 CE MET B 766 6.095 12.100 −54.463 1.00 67.19 ATOM 2737 N ASP B 767 4.678 7.412 −50.966 1.00 64.47 ATOM 2738 CA ASP B 767 3.642 7.109 −49.997 1.00 63.79 ATOM 2739 C ASP B 767 4.142 7.370 −48.587 1.00 61.82 ATOM 2740 O ASP B 767 3.420 7.922 −47.761 1.00 61.10 ATOM 2741 CB ASP B 767 3.186 5.660 −50.146 1.00 67.06 ATOM 2742 CG ASP B 767 2.150 5.490 −51.246 1.00 70.14 ATOM 2743 OD1 ASP B 767 1.000 5.939 −51.059 1.00 71.60 ATOM 2744 OD2 ASP B 767 2.484 4.917 −52.304 1.00 73.46 ATOM 2745 N GLU B 768 5.385 6.984 −48.320 1.00 60.15 ATOM 2746 CA GLU B 768 5.978 7.194 −47.008 1.00 58.81 ATOM 2747 C GLU B 768 6.184 8.689 −46.770 1.00 57.14 ATOM 2748 O GLU B 768 6.001 9.184 −45.654 1.00 54.76 ATOM 2749 CB GLU B 768 7.319 6.459 −46.906 1.00 61.07 ATOM 2750 CG GLU B 768 7.904 6.444 −45.495 1.00 64.70 ATOM 2751 CD GLU B 768 7.060 5.642 −44.506 1.00 66.61 ATOM 2752 OE1 GLU B 768 7.238 5.825 −43.283 1.00 68.31 ATOM 2753 OE2 GLU B 768 6.227 4.823 −44.948 1.00 66.65 ATOM 2754 N ALA B 769 6.553 9.405 −47.829 1.00 55.28 ATOM 2755 CA ALA B 769 6.773 10.841 −47.736 1.00 54.43 ATOM 2756 C ALA B 769 5.491 11.555 −47.326 1.00 54.12 ATOM 2757 O ALA B 769 5.535 12.625 −46.717 1.00 56.14 ATOM 2758 CB ALA B 769 7.274 11.385 −49.065 1.00 53.75 ATOM 2759 N LEU B 770 4.346 10.970 −47.657 1.00 52.05 ATOM 2760 CA LEU B 770 3.077 11.576 −47.287 1.00 51.69 ATOM 2761 C LEU B 770 2.921 11.494 −45.774 1.00 51.45 ATOM 2762 O LEU B 770 2.470 12.440 −45.125 1.00 52.01 ATOM 2763 CB LEU B 770 1.910 10.864 −47.991 1.00 52.43 ATOM 2764 CG LEU B 770 0.511 11.393 −47.636 1.00 53.86 ATOM 2765 CD1 LEU B 770 −0.417 11.306 −48.839 1.00 54.92 ATOM 2766 CD2 LEU B 770 −0.041 10.608 −46.450 1.00 52.30 ATOM 2767 N ILE B 771 3.307 10.357 −45.211 1.00 50.57 ATOM 2768 CA ILE B 771 3.216 10.175 −43.775 1.00 50.50 ATOM 2769 C ILE B 771 4.203 11.092 −43.060 1.00 50.19 ATOM 2770 O ILE B 771 3.883 11.700 −42.047 1.00 51.29 ATOM 2771 CB ILE B 771 3.511 8.726 −43.377 1.00 50.14 ATOM 2772 CG1 ILE B 771 2.554 7.778 −44.105 1.00 51.79 ATOM 2773 CG2 ILE B 771 3.340 8.569 −41.885 1.00 48.70 ATOM 2774 CD1 ILE B 771 1.078 8.018 −43.775 1.00 51.92 ATOM 2775 N MET B 772 5.409 11.197 −43.587 1.00 50.96 ATOM 2776 CA MET B 772 6.395 12.056 −42.962 1.00 52.41 ATOM 2777 C MET B 772 5.918 13.499 −42.960 1.00 53.45 ATOM 2778 O MET B 772 6.222 14.262 −42.053 1.00 56.84 ATOM 2779 CB MET B 772 7.727 11.960 −43.698 1.00 51.86 ATOM 2780 CG MET B 772 8.323 10.581 −43.694 1.00 51.45 ATOM 2781 SD MET B 772 9.869 10.566 −44.572 1.00 54.95 ATOM 2782 CE MET B 772 10.510 8.976 −44.043 1.00 57.12 ATOM 2783 N ALA B 773 5.156 13.875 −43.971 1.00 53.69 ATOM 2784 CA ALA B 773 4.680 15.240 −44.048 1.00 53.73 ATOM 2785 C ALA B 773 3.350 15.455 −43.331 1.00 53.40 ATOM 2786 O ALA B 773 2.955 16.588 −43.076 1.00 54.15 ATOM 2787 CB ALA B 773 4.567 15.651 −45.512 1.00 55.36 ATOM 2788 N SER B 774 2.653 14.380 −42.995 1.00 53.47 ATOM 2789 CA SER B 774 1.370 14.536 −42.321 1.00 54.15 ATOM 2790 C SER B 774 1.499 14.673 −40.805 1.00 54.10 ATOM 2791 O SER B 774 0.512 14.933 −40.126 1.00 55.42 ATOM 2792 CB SER B 774 0.457 13.352 −42.637 1.00 54.46 ATOM 2793 OG SER B 774 0.363 13.121 −44.027 1.00 57.39 ATOM 2794 N MET B 775 2.705 14.509 −40.275 1.00 53.87 ATOM 2795 CA MET B 775 2.924 14.594 −38.830 1.00 54.89 ATOM 2796 C MET B 775 2.843 15.992 −38.190 1.00 54.27 ATOM 2797 O MET B 775 3.665 16.858 −38.460 1.00 54.83 ATOM 2798 CB MET B 775 4.265 13.946 −38.496 1.00 55.60 ATOM 2799 CG MET B 775 4.357 12.524 −39.000 1.00 57.72 ATOM 2800 SD MET B 775 2.881 11.559 −38.576 1.00 63.74 ATOM 2801 CE MET B 775 3.577 10.256 −37.670 1.00 57.19 ATOM 2802 N ASP B 776 1.853 16.194 −37.323 1.00 54.06 ATOM 2803 CA ASP B 776 1.660 17.475 −36.645 1.00 53.45 ATOM 2804 C ASP B 776 1.627 17.322 −35.119 1.00 52.22 ATOM 2805 O ASP B 776 0.565 17.293 −34.493 1.00 51.95 ATOM 2806 CB ASP B 776 0.369 18.136 −37.133 1.00 55.05 ATOM 2807 CG ASP B 776 0.193 19.550 −36.595 1.00 57.95 ATOM 2808 OD1 ASP B 776 1.211 20.168 −36.195 1.00 56.53 ATOM 2809 OD2 ASP B 776 −0.961 20.046 −36.589 1.00 56.88 ATOM 2810 N HIS B 777 2.810 17.234 −34.529 1.00 50.34 ATOM 2811 CA HIS B 777 2.948 17.073 −33.094 1.00 47.37 ATOM 2812 C HIS B 777 4.238 17.764 −32.718 1.00 47.49 ATOM 2813 O HIS B 777 5.264 17.580 −33.374 1.00 45.96 ATOM 2814 CB HIS B 777 3.009 15.589 −32.737 1.00 45.58 ATOM 2815 CG HIS B 777 3.097 15.319 −31.268 1.00 45.70 ATOM 2816 ND1 HIS B 777 4.262 15.481 −30.549 1.00 46.20 ATOM 2817 CD2 HIS B 777 2.168 14.882 −30.386 1.00 44.55 ATOM 2818 CE1 HIS B 777 4.048 15.154 −29.287 1.00 44.22 ATOM 2819 NE2 HIS B 777 2.785 14.786 −29.162 1.00 46.79 ATOM 2820 N PRO B 778 4.204 18.572 −31.649 1.00 48.64 ATOM 2821 CA PRO B 778 5.382 19.308 −31.183 1.00 48.65 ATOM 2822 C PRO B 778 6.636 18.467 −30.938 1.00 48.69 ATOM 2823 O PRO B 778 7.755 18.986 −30.992 1.00 50.23 ATOM 2824 CB PRO B 778 4.871 20.020 −29.924 1.00 48.43 ATOM 2825 CG PRO B 778 3.796 19.118 −29.435 1.00 48.56 ATOM 2826 CD PRO B 778 3.089 18.707 −30.694 1.00 47.48 ATOM 2827 N HIS B 779 6.479 17.169 −30.708 1.00 47.19 ATOM 2828 CA HIS B 779 7.666 16.366 −30.468 1.00 46.69 ATOM 2829 C HIS B 779 8.062 15.405 −31.589 1.00 46.92 ATOM 2830 O HIS B 779 8.806 14.438 −31.387 1.00 45.42 ATOM 2831 CB HIS B 779 7.543 15.680 −29.108 1.00 43.27 ATOM 2832 CG HIS B 779 7.436 16.657 −27.979 1.00 42.66 ATOM 2833 ND1 HIS B 779 8.325 17.699 −27.821 1.00 41.28 ATOM 2834 CD2 HIS B 779 6.504 16.808 −27.010 1.00 42.33 ATOM 2835 CE1 HIS B 779 7.940 18.453 −26.808 1.00 42.15 ATOM 2836 NE2 HIS B 779 6.837 17.935 −26.298 1.00 39.93 ATOM 2837 N LEU B 780 7.583 15.711 −32.788 1.00 46.23 ATOM 2838 CA LEU B 780 7.920 14.935 −33.968 1.00 46.87 ATOM 2839 C LEU B 780 8.316 15.921 −35.056 1.00 47.73 ATOM 2840 O LEU B 780 7.772 17.024 −35.145 1.00 48.06 ATOM 2841 CB LEU B 780 6.730 14.107 −34.436 1.00 45.91 ATOM 2842 CG LEU B 780 6.235 12.985 −33.527 1.00 47.10 ATOM 2843 CD1 LEU B 780 5.096 12.287 −34.244 1.00 48.53 ATOM 2844 CD2 LEU B 780 7.349 11.987 −33.216 1.00 46.79 ATOM 2845 N VAL B 781 9.277 15.540 −35.878 1.00 48.83 ATOM 2846 CA VAL B 781 9.691 16.432 −36.944 1.00 51.89 ATOM 2847 C VAL B 781 8.710 16.336 −38.104 1.00 53.37 ATOM 2848 O VAL B 781 7.995 15.349 −38.258 1.00 52.89 ATOM 2849 CB VAL B 781 11.109 16.094 −37.444 1.00 50.59 ATOM 2850 CG1 VAL B 781 12.078 16.089 −36.266 1.00 49.98 ATOM 2851 CG2 VAL B 781 11.107 14.757 −38.152 1.00 48.87 ATOM 2852 N ARG B 782 8.675 17.382 −38.914 1.00 56.80 ATOM 2853 CA ARG B 782 7.793 17.423 −40.070 1.00 59.13 ATOM 2854 C ARG B 782 8.643 17.636 −41.316 1.00 58.23 ATOM 2855 O ARG B 782 9.646 18.364 −41.293 1.00 57.16 ATOM 2856 CB ARG B 782 6.784 18.562 −39.923 1.00 61.42 ATOM 2857 CG ARG B 782 5.654 18.537 −40.920 1.00 66.10 ATOM 2858 CD ARG B 782 4.579 19.529 −40.496 1.00 72.64 ATOM 2859 NE ARG B 782 3.401 19.499 −41.364 1.00 77.10 ATOM 2860 CZ ARG B 782 2.293 20.207 −41.147 1.00 78.91 ATOM 2861 NH1 ARG B 782 2.205 21.003 −40.085 1.00 78.69 ATOM 2862 NH2 ARG B 782 1.273 20.129 −41.997 1.00 80.27 ATOM 2863 N LEU B 783 8.247 16.980 −42.397 1.00 56.30 ATOM 2864 CA LEU B 783 8.958 17.102 −43.654 1.00 55.96 ATOM 2865 C LEU B 783 8.383 18.309 −44.374 1.00 54.57 ATOM 2866 O LEU B 783 7.175 18.392 −44.573 1.00 56.01 ATOM 2867 CB LEU B 783 8.745 15.839 −44.486 1.00 57.21 ATOM 2868 CG LEU B 783 9.516 15.702 −45.795 1.00 55.26 ATOM 2869 CD1 LEU B 783 11.009 15.669 −45.514 1.00 56.03 ATOM 2870 CD2 LEU B 783 9.080 14.436 −46.485 1.00 55.49 ATOM 2871 N LEU B 784 9.242 19.250 −44.747 1.00 54.51 ATOM 2872 CA LEU B 784 8.788 20.450 −45.444 1.00 54.07 ATOM 2873 C LEU B 784 8.526 20.132 −46.903 1.00 52.39 ATOM 2874 O LEU B 784 7.471 20.466 −47.443 1.00 52.32 ATOM 2875 CB LEU B 784 9.832 21.564 −45.340 1.00 54.48 ATOM 2876 CG LEU B 784 10.072 22.091 −43.920 1.00 57.09 ATOM 2877 CD1 LEU B 784 11.245 23.059 −43.919 1.00 57.21 ATOM 2878 CD2 LEU B 784 8.810 22.765 −43.393 1.00 56.32 ATOM 2879 N GLY B 785 9.488 19.470 −47.535 1.00 50.88 ATOM 2880 CA GLY B 785 9.325 19.128 −48.931 1.00 48.30 ATOM 2881 C GLY B 785 10.255 18.057 −49.460 1.00 48.59 ATOM 2882 O GLY B 785 11.104 17.513 −48.755 1.00 46.94 ATOM 2883 N VAL B 786 10.077 17.750 −50.733 1.00 48.89 ATOM 2884 CA VAL B 786 10.891 16.755 −51.381 1.00 49.74 ATOM 2885 C VAL B 786 11.370 17.317 −52.707 1.00 51.57 ATOM 2886 O VAL B 786 10.638 18.059 −53.385 1.00 50.67 ATOM 2887 CB VAL B 786 10.083 15.468 −51.640 1.00 50.26 ATOM 2888 CG1 VAL B 786 10.931 14.473 −52.414 1.00 50.36 ATOM 2889 CG2 VAL B 786 9.638 14.858 −50.320 1.00 49.86 ATOM 2890 N CYS B 787 12.609 16.983 −53.058 1.00 50.94 ATOM 2891 CA CYS B 787 13.187 17.414 −54.316 1.00 51.41 ATOM 2892 C CYS B 787 13.398 16.134 −55.113 1.00 51.83 ATOM 2893 O CYS B 787 14.017 15.193 −54.627 1.00 51.13 ATOM 2894 CB CYS B 787 14.515 18.135 −54.089 1.00 52.49 ATOM 2895 SG CYS B 787 15.263 18.700 −55.644 1.00 57.81 ATOM 2896 N LEU B 788 12.891 16.105 −56.339 1.00 54.13 ATOM 2897 CA LEU B 788 12.975 14.915 −57.173 1.00 57.19 ATOM 2898 C LEU B 788 14.242 14.704 −57.992 1.00 61.05 ATOM 2899 O LEU B 788 14.481 13.599 −58.479 1.00 61.41 ATOM 2900 CB LEU B 788 11.751 14.864 −58.089 1.00 55.35 ATOM 2901 CG LEU B 788 10.426 14.802 −57.311 1.00 56.39 ATOM 2902 CD1 LEU B 788 9.251 14.950 −58.250 1.00 55.47 ATOM 2903 CD2 LEU B 788 10.334 13.487 −56.548 1.00 55.46 ATOM 2904 N SER B 789 15.066 15.737 −58.146 1.00 64.33 ATOM 2905 CA SER B 789 16.285 15.582 −58.938 1.00 66.33 ATOM 2906 C SER B 789 17.520 16.071 −58.192 1.00 66.73 ATOM 2907 O SER B 789 17.424 16.955 −57.336 1.00 66.88 ATOM 2908 CB SER B 789 16.141 16.337 −60.264 1.00 67.97 ATOM 2909 OG SER B 789 17.099 15.892 −61.214 1.00 72.18 ATOM 2910 N PRO B 790 18.697 15.474 −58.477 1.00 67.24 ATOM 2911 CA PRO B 790 18.941 14.388 −59.439 1.00 66.95 ATOM 2912 C PRO B 790 18.245 13.123 −58.965 1.00 67.17 ATOM 2913 O PRO B 790 17.782 12.298 −59.757 1.00 66.12 ATOM 2914 CB PRO B 790 20.454 14.242 −59.407 1.00 66.69 ATOM 2915 CG PRO B 790 20.768 14.555 −57.969 1.00 66.95 ATOM 2916 CD PRO B 790 19.933 15.791 −57.739 1.00 66.62 ATOM 2917 N THR B 791 18.209 12.987 −57.646 1.00 66.82 ATOM 2918 CA THR B 791 17.565 11.869 −56.986 1.00 66.98 ATOM 2919 C THR B 791 16.862 12.492 −55.791 1.00 65.80 ATOM 2920 O THR B 791 17.173 13.617 −55.392 1.00 64.64 ATOM 2921 CB THR B 791 18.583 10.805 −56.503 1.00 69.05 ATOM 2922 OG1 THR B 791 19.435 11.370 −55.496 1.00 69.07 ATOM 2923 CG2 THR B 791 19.431 10.306 −57.679 1.00 69.29 ATOM 2924 N ILE B 792 15.920 11.748 −55.229 1.00 64.46 ATOM 2925 CA ILE B 792 15.117 12.198 −54.103 1.00 62.56 ATOM 2926 C ILE B 792 15.841 12.710 −52.871 1.00 61.32 ATOM 2927 O ILE B 792 16.659 12.011 −52.283 1.00 62.26 ATOM 2928 CB ILE B 792 14.152 11.093 −53.677 1.00 60.97 ATOM 2929 CG1 ILE B 792 13.035 10.988 −54.710 1.00 61.00 ATOM 2930 CG2 ILE B 792 13.616 11.383 −52.311 1.00 58.92 ATOM 2931 CD1 ILE B 792 12.063 9.871 −54.469 1.00 65.86 ATOM 2932 N GLN B 793 15.510 13.938 −52.483 1.00 60.22 ATOM 2933 CA GLN B 793 16.103 14.566 −51.310 1.00 60.54 ATOM 2934 C GLN B 793 14.994 14.972 −50.352 1.00 59.77 ATOM 2935 O GLN B 793 13.964 15.522 −50.766 1.00 59.02 ATOM 2936 CB GLN B 793 16.897 15.817 −51.694 1.00 61.88 ATOM 2937 CG GLN B 793 17.928 15.613 −52.782 1.00 64.34 ATOM 2938 CD GLN B 793 18.587 16.913 −53.200 1.00 65.85 ATOM 2939 OE1 GLN B 793 19.084 17.033 −54.317 1.00 67.77 ATOM 2940 NE2 GLN B 793 18.601 17.893 −52.299 1.00 66.10 ATOM 2941 N LEU B 794 15.213 14.697 −49.072 1.00 58.48 ATOM 2942 CA LEU B 794 14.250 15.036 −48.042 1.00 57.14 ATOM 2943 C LEU B 794 14.689 16.346 −47.414 1.00 57.64 ATOM 2944 O LEU B 794 15.859 16.531 −47.093 1.00 57.64 ATOM 2945 CB LEU B 794 14.187 13.922 −46.992 1.00 55.84 ATOM 2946 CG LEU B 794 13.804 12.529 −47.515 1.00 54.27 ATOM 2947 CD1 LEU B 794 13.456 11.624 −46.344 1.00 53.66 ATOM 2948 CD2 LEU B 794 12.616 12.627 −48.449 1.00 53.08 ATOM 2949 N VAL B 795 13.746 17.264 −47.258 1.00 59.07 ATOM 2950 CA VAL B 795 14.047 18.567 −46.690 1.00 59.85 ATOM 2951 C VAL B 795 13.222 18.812 −45.435 1.00 62.17 ATOM 2952 O VAL B 795 11.987 18.855 −45.472 1.00 61.88 ATOM 2953 CB VAL B 795 13.774 19.697 −47.714 1.00 58.39 ATOM 2954 CG1 VAL B 795 14.231 21.040 −47.157 1.00 58.05 ATOM 2955 CG2 VAL B 795 14.495 19.394 −49.014 1.00 58.45 ATOM 2956 N THR B 796 13.931 18.969 −44.323 1.00 63.79 ATOM 2957 CA THR B 796 13.311 19.210 −43.034 1.00 65.36 ATOM 2958 C THR B 796 13.869 20.476 −42.436 1.00 66.46 ATOM 2959 O THR B 796 14.993 20.890 −42.747 1.00 66.26 ATOM 2960 CB THR B 796 13.606 18.077 −42.033 1.00 65.06 ATOM 2961 OG1 THR B 796 13.043 16.852 −42.509 1.00 68.33 ATOM 2962 CG2 THR B 796 13.007 18.401 −40.672 1.00 66.50 ATOM 2963 N GLN B 797 13.068 21.090 −41.574 1.00 66.67 ATOM 2964 CA GLN B 797 13.488 22.284 −40.884 1.00 66.57 ATOM 2965 C GLN B 797 14.690 21.827 −40.085 1.00 66.07 ATOM 2966 O GLN B 797 14.680 20.741 −39.501 1.00 65.39 ATOM 2967 CB GLN B 797 12.393 22.758 −39.935 1.00 67.57 ATOM 2968 CG GLN B 797 12.673 24.081 −39.263 1.00 70.20 ATOM 2969 CD GLN B 797 11.514 24.526 −38.399 1.00 73.88 ATOM 2970 OE1 GLN B 797 11.403 24.140 −37.230 1.00 75.03 ATOM 2971 NE2 GLN B 797 10.623 25.327 −38.979 1.00 74.39 ATOM 2972 N LEU B 798 15.737 22.638 −40.083 1.00 66.31 ATOM 2973 CA LEU B 798 16.931 22.303 −39.333 1.00 65.46 ATOM 2974 C LEU B 798 16.672 22.549 −37.851 1.00 66.20 ATOM 2975 O LEU B 798 15.902 23.441 −37.476 1.00 65.77 ATOM 2976 CB LEU B 798 18.097 23.170 −39.791 1.00 64.87 ATOM 2977 CG LEU B 798 19.410 22.965 −39.045 1.00 65.11 ATOM 2978 CD1 LEU B 798 19.933 21.554 −39.290 1.00 64.89 ATOM 2979 CD2 LEU B 798 20.411 23.999 −39.516 1.00 64.74 ATOM 2980 N MET B 799 17.296 21.733 −37.011 1.00 66.39 ATOM 2981 CA MET B 799 17.169 21.885 −35.571 1.00 65.45 ATOM 2982 C MET B 799 18.506 22.465 −35.113 1.00 65.57 ATOM 2983 O MET B 799 19.547 21.798 −35.162 1.00 64.60 ATOM 2984 CB MET B 799 16.881 20.536 −34.911 1.00 64.87 ATOM 2985 CG MET B 799 15.491 19.990 −35.216 1.00 64.16 ATOM 2986 SD MET B 799 14.163 21.040 −34.582 1.00 65.40 ATOM 2987 CE MET B 799 13.635 21.891 −36.058 1.00 64.20 ATOM 2988 N PRO B 800 18.486 23.730 −34.669 1.00 65.90 ATOM 2989 CA PRO B 800 19.652 24.484 −34.196 1.00 65.62 ATOM 2990 C PRO B 800 20.591 23.765 −33.239 1.00 65.08 ATOM 2991 O PRO B 800 21.805 23.817 −33.412 1.00 64.72 ATOM 2992 CB PRO B 800 19.025 25.731 −33.566 1.00 66.58 ATOM 2993 CG PRO B 800 17.699 25.239 −33.092 1.00 66.63 ATOM 2994 CD PRO B 800 17.241 24.410 −34.269 1.00 66.65 ATOM 2995 N HIS B 801 20.044 23.088 −32.237 1.00 63.99 ATOM 2996 CA HIS B 801 20.892 22.408 −31.277 1.00 62.97 ATOM 2997 C HIS B 801 21.310 20.988 −31.636 1.00 61.86 ATOM 2998 O HIS B 801 21.843 20.257 −30.804 1.00 63.07 ATOM 2999 CB HIS B 801 20.238 22.471 −29.900 1.00 64.77 ATOM 3000 CG HIS B 801 20.298 23.836 −29.283 1.00 66.40 ATOM 3001 ND1 HIS B 801 21.486 24.432 −28.909 1.00 65.11 ATOM 3002 CD2 HIS B 801 19.324 24.740 −29.016 1.00 66.09 ATOM 3003 CE1 HIS B 801 21.240 25.641 −28.439 1.00 64.78 ATOM 3004 NE2 HIS B 801 19.936 25.853 −28.492 1.00 65.44 ATOM 3005 N GLY B 802 21.090 20.607 −32.886 1.00 60.15 ATOM 3006 CA GLY B 802 21.490 19.289 −33.331 1.00 57.51 ATOM 3007 C GLY B 802 20.901 18.064 −32.650 1.00 56.35 ATOM 3008 O GLY B 802 19.810 18.086 −32.075 1.00 53.17 ATOM 3009 N CYS B 803 21.660 16.978 −32.735 1.00 56.15 ATOM 3010 CA CYS B 803 21.277 15.688 −32.190 1.00 55.11 ATOM 3011 C CYS B 803 21.445 15.568 −30.682 1.00 55.33 ATOM 3012 O CYS B 803 22.491 15.911 −30.128 1.00 54.75 ATOM 3013 CB CYS B 803 22.074 14.594 −32.899 1.00 55.30 ATOM 3014 SG CYS B 803 21.743 14.518 −34.697 1.00 60.15 ATOM 3015 N LEU B 804 20.396 15.066 −30.031 1.00 54.33 ATOM 3016 CA LEU B 804 20.376 14.883 −28.588 1.00 53.12 ATOM 3017 C LEU B 804 21.534 14.014 −28.089 1.00 52.92 ATOM 3018 O LEU B 804 22.177 14.328 −27.088 1.00 51.69 ATOM 3019 CB LEU B 804 19.043 14.266 −28.168 1.00 52.44 ATOM 3020 CG LEU B 804 18.815 14.078 −26.666 1.00 50.62 ATOM 3021 CD1 LEU B 804 18.967 15.417 −25.974 1.00 51.38 ATOM 3022 CD2 LEU B 804 17.428 13.491 −26.413 1.00 49.29 ATOM 3023 N LEU B 805 21.801 12.920 −28.782 1.00 52.39 ATOM 3024 CA LEU B 805 22.888 12.053 −28.373 1.00 54.68 ATOM 3025 C LEU B 805 24.161 12.863 −28.138 1.00 57.25 ATOM 3026 O LEU B 805 24.918 12.604 −27.200 1.00 56.94 ATOM 3027 CB LEU B 805 23.156 10.998 −29.438 1.00 52.27 ATOM 3028 CG LEU B 805 24.380 10.169 −29.080 1.00 51.83 ATOM 3029 CD1 LEU B 805 24.151 9.471 −27.737 1.00 50.62 ATOM 3030 CD2 LEU B 805 24.660 9.179 −30.182 1.00 53.24 ATOM 3031 N GLU B 806 24.387 13.844 −29.006 1.00 60.22 ATOM 3032 CA GLU B 806 25.558 14.705 −28.919 1.00 62.56 ATOM 3033 C GLU B 806 25.351 15.761 −27.836 1.00 60.94 ATOM 3034 O GLU B 806 26.233 16.013 −27.018 1.00 60.73 ATOM 3035 CB GLU B 806 25.804 15.395 −30.267 1.00 67.71 ATOM 3036 CG GLU B 806 25.695 14.471 −31.488 1.00 75.24 ATOM 3037 CD GLU B 806 25.922 15.212 −32.804 1.00 79.21 ATOM 3038 OE1 GLU B 806 25.254 16.251 −33.026 1.00 81.47 ATOM 3039 OE2 GLU B 806 26.762 14.758 −33.615 1.00 79.92 ATOM 3040 N TYR B 807 24.173 16.371 −27.832 1.00 59.29 ATOM 3041 CA TYR B 807 23.856 17.400 −26.860 1.00 59.19 ATOM 3042 C TYR B 807 24.157 16.981 −25.424 1.00 59.38 ATOM 3043 O TYR B 807 24.822 17.708 −24.700 1.00 58.77 ATOM 3044 CB TYR B 807 22.391 17.784 −26.966 1.00 59.99 ATOM 3045 CG TYR B 807 22.053 19.071 −26.262 1.00 60.81 ATOM 3046 CD1 TYR B 807 22.227 20.300 −26.897 1.00 61.13 ATOM 3047 CD2 TYR B 807 21.546 19.064 −24.966 1.00 61.33 ATOM 3048 CE1 TYR B 807 21.899 21.489 −26.265 1.00 61.63 ATOM 3049 CE2 TYR B 807 21.215 20.252 −24.319 1.00 62.89 ATOM 3050 CZ TYR B 807 21.392 21.460 −24.977 1.00 62.83 ATOM 3051 OH TYR B 807 21.035 22.630 −24.354 1.00 64.52 ATOM 3052 N VAL B 808 23.671 15.819 −25.002 1.00 60.10 ATOM 3053 CA VAL B 808 23.927 15.382 −23.630 1.00 62.18 ATOM 3054 C VAL B 808 25.398 15.164 −23.325 1.00 63.86 ATOM 3055 O VAL B 808 25.855 15.480 −22.235 1.00 64.12 ATOM 3056 CB VAL B 808 23.176 14.073 −23.257 1.00 60.51 ATOM 3057 CG1 VAL B 808 21.704 14.344 −23.088 1.00 59.12 ATOM 3058 CG2 VAL B 808 23.417 13.015 −24.310 1.00 60.89 ATOM 3059 N HIS B 809 26.147 14.624 −24.273 1.00 67.06 ATOM 3060 CA HIS B 809 27.555 14.383 −24.014 1.00 70.40 ATOM 3061 C HIS B 809 28.269 15.679 −23.658 1.00 70.99 ATOM 3062 O HIS B 809 28.886 15.797 −22.602 1.00 72.12 ATOM 3063 CB HIS B 809 28.236 13.746 −25.226 1.00 73.29 ATOM 3064 CG HIS B 809 29.639 13.294 −24.956 1.00 76.84 ATOM 3065 ND1 HIS B 809 29.937 12.293 −24.056 1.00 77.14 ATOM 3066 CD2 HIS B 809 30.826 13.724 −25.447 1.00 77.99 ATOM 3067 CE1 HIS B 809 31.247 12.126 −24.005 1.00 78.08 ATOM 3068 NE2 HIS B 809 31.809 12.982 −24.839 1.00 78.17 ATOM 3069 N GLU B 810 28.162 16.660 −24.537 1.00 71.44 ATOM 3070 CA GLU B 810 28.827 17.928 −24.322 1.00 72.20 ATOM 3071 C GLU B 810 28.320 18.741 −23.141 1.00 72.35 ATOM 3072 O GLU B 810 29.121 19.284 −22.378 1.00 72.42 ATOM 3073 CB GLU B 810 28.760 18.741 −25.604 1.00 74.24 ATOM 3074 CG GLU B 810 29.503 18.067 −26.746 1.00 76.99 ATOM 3075 CD GLU B 810 29.191 18.694 −28.082 1.00 80.01 ATOM 3076 OE1 GLU B 810 29.408 19.918 −28.231 1.00 81.26 ATOM 3077 OE2 GLU B 810 28.726 17.961 −28.982 1.00 80.87 ATOM 3078 N HIS B 811 27.001 18.822 −22.976 1.00 72.11 ATOM 3079 CA HIS B 811 26.427 19.588 −21.869 1.00 71.84 ATOM 3080 C HIS B 811 26.168 18.752 −20.624 1.00 71.80 ATOM 3081 O HIS B 811 25.302 19.096 −19.820 1.00 70.61 ATOM 3082 CB HIS B 811 25.115 20.252 −22.286 1.00 71.49 ATOM 3083 CG HIS B 811 25.243 21.157 −23.468 1.00 71.98 ATOM 3084 ND1 HIS B 811 25.549 20.695 −24.729 1.00 73.94 ATOM 3085 CD2 HIS B 811 25.085 22.496 −23.586 1.00 72.36 ATOM 3086 CE1 HIS B 811 25.571 21.709 −25.575 1.00 74.46 ATOM 3087 NE2 HIS B 811 25.293 22.813 −24.907 1.00 74.62 ATOM 3088 N LYS B 812 26.917 17.665 −20.460 1.00 73.21 ATOM 3089 CA LYS B 812 26.736 16.793 −19.300 1.00 75.11 ATOM 3090 C LYS B 812 26.604 17.575 −18.001 1.00 75.97 ATOM 3091 O LYS B 812 25.592 17.499 −17.305 1.00 75.98 ATOM 3092 CB LYS B 812 27.901 15.805 −19.157 1.00 74.11 ATOM 3093 CG LYS B 812 27.887 15.118 −17.799 1.00 74.38 ATOM 3094 CD LYS B 812 28.809 13.917 −17.690 1.00 73.97 ATOM 3095 CE LYS B 812 28.613 13.265 −16.322 1.00 72.70 ATOM 3096 NZ LYS B 812 29.394 12.015 −16.154 1.00 73.35 ATOM 3097 N ASP B 813 27.642 18.330 −17.682 1.00 77.79 ATOM 3098 CA ASP B 813 27.668 19.119 −16.463 1.00 79.44 ATOM 3099 C ASP B 813 26.644 20.256 −16.500 1.00 79.12 ATOM 3100 O ASP B 813 26.706 21.185 −15.699 1.00 79.20 ATOM 3101 CB ASP B 813 29.085 19.659 −16.258 1.00 81.16 ATOM 3102 CG ASP B 813 30.154 18.594 −16.504 1.00 83.14 ATOM 3103 OD1 ASP B 813 30.044 17.498 −15.912 1.00 82.59 ATOM 3104 OD2 ASP B 813 31.101 18.845 −17.288 1.00 84.71 ATOM 3105 N ASN B 814 25.688 20.159 −17.421 1.00 78.87 ATOM 3106 CA ASN B 814 24.653 21.178 −17.570 1.00 77.92 ATOM 3107 C ASN B 814 23.247 20.591 −17.474 1.00 75.00 ATOM 3108 O ASN B 814 22.278 21.320 −17.278 1.00 73.54 ATOM 3109 CB ASN B 814 24.807 21.875 −18.925 1.00 83.27 ATOM 3110 CG ASN B 814 23.809 23.011 −19.123 1.00 87.37 ATOM 3111 OD1 ASN B 814 23.599 23.487 −20.248 1.00 89.03 ATOM 3112 ND2 ASN B 814 23.200 23.462 −18.027 1.00 88.12 ATOM 3113 N ILE B 815 23.136 19.274 −17.610 1.00 72.06 ATOM 3114 CA ILE B 815 21.834 18.608 −17.567 1.00 68.21 ATOM 3115 C ILE B 815 21.335 18.306 −16.157 1.00 65.98 ATOM 3116 O ILE B 815 22.010 17.630 −15.374 1.00 66.13 ATOM 3117 CB ILE B 815 21.864 17.285 −18.361 1.00 67.26 ATOM 3118 CG1 ILE B 815 22.485 17.517 −19.738 1.00 66.10 ATOM 3119 CG2 ILE B 815 20.461 16.739 −18.512 1.00 66.10 ATOM 3120 CD1 ILE B 815 21.770 18.532 −20.565 1.00 65.00 ATOM 3121 N GLY B 816 20.139 18.806 −15.853 1.00 63.12 ATOM 3122 CA GLY B 816 19.534 18.592 −14.549 1.00 59.27 ATOM 3123 C GLY B 816 18.502 17.479 −14.584 1.00 57.42 ATOM 3124 O GLY B 816 18.077 17.046 −15.658 1.00 56.24 ATOM 3125 N SER B 817 18.081 17.013 −13.413 1.00 53.84 ATOM 3126 CA SER B 817 17.118 15.936 −13.375 1.00 51.45 ATOM 3127 C SER B 817 15.826 16.343 −14.067 1.00 50.87 ATOM 3128 O SER B 817 15.205 15.532 −14.746 1.00 51.59 ATOM 3129 CB SER B 817 16.841 15.493 −11.927 1.00 50.35 ATOM 3130 OG SER B 817 16.050 16.422 −11.214 1.00 48.83 ATOM 3131 N GLN B 818 15.426 17.597 −13.914 1.00 48.39 ATOM 3132 CA GLN B 818 14.189 18.046 −14.531 1.00 50.14 ATOM 3133 C GLN B 818 14.256 17.872 −16.048 1.00 50.37 ATOM 3134 O GLN B 818 13.397 17.234 −16.664 1.00 50.57 ATOM 3135 CB GLN B 818 13.931 19.509 −14.172 1.00 51.39 ATOM 3136 CG GLN B 818 12.530 20.005 −14.512 1.00 53.65 ATOM 3137 CD GLN B 818 12.304 21.465 −14.104 1.00 54.44 ATOM 3138 OE1 GLN B 818 13.090 22.354 −14.451 1.00 51.78 ATOM 3139 NE2 GLN B 818 11.223 21.711 −13.374 1.00 53.12 ATOM 3140 N LEU B 819 15.299 18.439 −16.636 1.00 49.58 ATOM 3141 CA LEU B 819 15.542 18.376 −18.071 1.00 48.96 ATOM 3142 C LEU B 819 15.433 16.942 −18.617 1.00 48.91 ATOM 3143 O LEU B 819 14.665 16.680 −19.537 1.00 47.63 ATOM 3144 CB LEU B 819 16.937 18.931 −18.342 1.00 49.33 ATOM 3145 CG LEU B 819 17.233 19.667 −19.638 1.00 50.99 ATOM 3146 CD1 LEU B 819 16.180 20.729 −19.883 1.00 51.26 ATOM 3147 CD2 LEU B 819 18.620 20.284 −19.528 1.00 48.42 ATOM 3148 N LEU B 820 16.207 16.027 −18.036 1.00 48.12 ATOM 3149 CA LEU B 820 16.232 14.627 −18.448 1.00 47.03 ATOM 3150 C LEU B 820 14.908 13.879 −18.355 1.00 47.74 ATOM 3151 O LEU B 820 14.621 13.036 −19.210 1.00 46.11 ATOM 3152 CB LEU B 820 17.284 13.865 −17.648 1.00 46.94 ATOM 3153 CG LEU B 820 18.733 14.082 −18.069 1.00 46.17 ATOM 3154 CD1 LEU B 820 19.655 13.512 −17.010 1.00 48.56 ATOM 3155 CD2 LEU B 820 18.982 13.429 −19.417 1.00 47.04 ATOM 3156 N LEU B 821 14.119 14.159 −17.315 1.00 47.54 ATOM 3157 CA LEU B 821 12.818 13.508 −17.140 1.00 47.15 ATOM 3158 C LEU B 821 11.781 14.084 −18.094 1.00 47.22 ATOM 3159 O LEU B 821 10.822 13.407 −18.463 1.00 48.21 ATOM 3160 CB LEU B 821 12.311 13.667 −15.712 1.00 46.22 ATOM 3161 CG LEU B 821 12.974 12.829 −14.621 1.00 48.11 ATOM 3162 CD1 LEU B 821 12.444 13.272 −13.264 1.00 46.19 ATOM 3163 CD2 LEU B 821 12.685 11.353 −14.844 1.00 46.08 ATOM 3164 N ASN B 822 11.970 15.336 −18.489 1.00 47.10 ATOM 3165 CA ASN B 822 11.048 15.981 −19.415 1.00 48.36 ATOM 3166 C ASN B 822 11.311 15.539 −20.860 1.00 46.42 ATOM 3167 O ASN B 822 10.398 15.478 −21.678 1.00 46.12 ATOM 3168 CB ASN B 822 11.153 17.499 −19.263 1.00 52.20 ATOM 3169 CG ASN B 822 10.430 18.003 −18.020 1.00 56.94 ATOM 3170 OD1 ASN B 822 9.200 18.106 −18.005 1.00 60.36 ATOM 3171 ND2 ASN B 822 11.184 18.295 −16.966 1.00 58.16 ATOM 3172 N TRP B 823 12.560 15.220 −21.174 1.00 45.04 ATOM 3173 CA TRP B 823 12.878 14.746 −22.512 1.00 43.92 ATOM 3174 C TRP B 823 12.219 13.378 −22.647 1.00 43.43 ATOM 3175 O TRP B 823 11.667 13.026 −23.698 1.00 42.53 ATOM 3176 CB TRP B 823 14.390 14.597 −22.700 1.00 42.86 ATOM 3177 CG TRP B 823 15.149 15.901 −22.828 1.00 44.63 ATOM 3178 CD1 TRP B 823 14.654 17.109 −23.246 1.00 43.05 ATOM 3179 CD2 TRP B 823 16.553 16.098 −22.612 1.00 44.09 ATOM 3180 NE1 TRP B 823 15.664 18.036 −23.308 1.00 43.18 ATOM 3181 CE2 TRP B 823 16.840 17.445 −22.923 1.00 44.18 ATOM 3182 CE3 TRP B 823 17.599 15.264 −22.184 1.00 44.59 ATOM 3183 CZ2 TRP B 823 18.133 17.985 −22.818 1.00 44.47 ATOM 3184 CZ3 TRP B 823 18.886 15.803 −22.080 1.00 46.01 ATOM 3185 CH2 TRP B 823 19.139 17.154 −22.397 1.00 42.03 ATOM 3186 N CYS B 824 12.274 12.617 −21.560 1.00 41.79 ATOM 3187 CA CYS B 824 11.699 11.290 −21.535 1.00 42.66 ATOM 3188 C CYS B 824 10.243 11.359 −21.920 1.00 44.42 ATOM 3189 O CYS B 824 9.785 10.604 −22.778 1.00 45.73 ATOM 3190 CB CYS B 824 11.846 10.663 −20.144 1.00 43.86 ATOM 3191 SG CYS B 824 13.522 10.059 −19.758 1.00 43.47 ATOM 3192 N VAL B 825 9.521 12.278 −21.287 1.00 45.21 ATOM 3193 CA VAL B 825 8.100 12.455 −21.549 1.00 42.85 ATOM 3194 C VAL B 825 7.858 12.902 −22.979 1.00 42.45 ATOM 3195 O VAL B 825 6.970 12.394 −23.665 1.00 40.16 ATOM 3196 CB VAL B 825 7.486 13.495 −20.585 1.00 42.45 ATOM 3197 CG1 VAL B 825 6.062 13.834 −21.014 1.00 41.54 ATOM 3198 CG2 VAL B 825 7.488 12.948 −19.173 1.00 40.00 ATOM 3199 N GLN B 826 8.650 13.868 −23.423 1.00 43.25 ATOM 3200 CA GLN B 826 8.510 14.379 −24.776 1.00 43.45 ATOM 3201 C GLN B 826 8.769 13.251 −25.762 1.00 41.87 ATOM 3202 O GLN B 826 7.985 13.044 −26.685 1.00 42.00 ATOM 3203 CB GLN B 826 9.468 15.555 −25.000 1.00 42.33 ATOM 3204 CG GLN B 826 9.022 16.786 −24.250 1.00 44.18 ATOM 3205 CD GLN B 826 9.988 17.944 −24.348 1.00 44.47 ATOM 3206 OE1 GLN B 826 10.716 18.084 −25.321 1.00 43.53 ATOM 3207 NE2 GLN B 826 9.981 18.799 −23.335 1.00 47.99 ATOM 3208 N ILE B 827 9.845 12.498 −25.565 1.00 39.85 ATOM 3209 CA ILE B 827 10.093 11.406 −26.487 1.00 40.62 ATOM 3210 C ILE B 827 8.928 10.412 −26.458 1.00 41.30 ATOM 3211 O ILE B 827 8.459 9.988 −27.513 1.00 43.72 ATOM 3212 CB ILE B 827 11.402 10.662 −26.178 1.00 39.44 ATOM 3213 CG1 ILE B 827 12.578 11.636 −26.275 1.00 38.32 ATOM 3214 CG2 ILE B 827 11.583 9.500 −27.171 1.00 37.20 ATOM 3215 CD1 ILE B 827 13.934 11.012 −26.017 1.00 37.82 ATOM 3216 N ALA B 828 8.448 10.059 −25.266 1.00 38.63 ATOM 3217 CA ALA B 828 7.347 9.113 −25.146 1.00 40.14 ATOM 3218 C ALA B 828 6.043 9.649 −25.728 1.00 42.58 ATOM 3219 O ALA B 828 5.185 8.881 −26.177 1.00 43.82 ATOM 3220 CB ALA B 828 7.140 8.723 −23.692 1.00 40.67 ATOM 3221 N LYS B 829 5.873 10.963 −25.722 1.00 44.00 ATOM 3222 CA LYS B 829 4.647 11.525 −26.273 1.00 43.33 ATOM 3223 C LYS B 829 4.656 11.428 −27.795 1.00 43.62 ATOM 3224 O LYS B 829 3.640 11.094 −28.401 1.00 44.41 ATOM 3225 CB LYS B 829 4.461 12.971 −25.809 1.00 43.70 ATOM 3226 CG LYS B 829 3.810 13.088 −24.433 1.00 41.95 ATOM 3227 CD LYS B 829 3.641 14.542 −24.038 1.00 44.96 ATOM 3228 CE LYS B 829 2.871 14.679 −22.747 1.00 47.02 ATOM 3229 NZ LYS B 829 2.772 16.101 −22.347 1.00 49.90 ATOM 3230 N GLY B 830 5.803 11.704 −28.410 1.00 42.29 ATOM 3231 CA GLY B 830 5.897 11.603 −29.854 1.00 42.16 ATOM 3232 C GLY B 830 5.631 10.178 −30.327 1.00 42.55 ATOM 3233 O GLY B 830 4.952 9.958 −31.336 1.00 43.40 ATOM 3234 N MET B 831 6.178 9.202 −29.611 1.00 41.44 ATOM 3235 CA MET B 831 5.955 7.811 −29.972 1.00 43.60 ATOM 3236 C MET B 831 4.450 7.563 −29.842 1.00 43.46 ATOM 3237 O MET B 831 3.840 6.886 −30.670 1.00 42.80 ATOM 3238 CB MET B 831 6.748 6.867 −29.042 1.00 43.14 ATOM 3239 CG MET B 831 8.267 6.966 −29.199 1.00 42.68 ATOM 3240 SD MET B 831 8.809 6.840 −30.938 1.00 43.27 ATOM 3241 CE MET B 831 8.511 5.103 −31.247 1.00 44.19 ATOM 3242 N MET B 832 3.860 8.142 −28.802 1.00 42.18 ATOM 3243 CA MET B 832 2.433 8.006 −28.549 1.00 43.21 ATOM 3244 C MET B 832 1.641 8.454 −29.780 1.00 42.04 ATOM 3245 O MET B 832 0.683 7.793 −30.201 1.00 40.20 ATOM 3246 CB MET B 832 2.062 8.866 −27.347 1.00 46.91 ATOM 3247 CG MET B 832 0.984 8.297 −26.452 1.00 50.62 ATOM 3248 SD MET B 832 0.679 9.445 −25.093 1.00 58.47 ATOM 3249 CE MET B 832 1.936 8.941 −24.018 1.00 53.62 ATOM 3250 N TYR B 833 2.066 9.581 −30.349 1.00 40.89 ATOM 3251 CA TYR B 833 1.439 10.157 −31.523 1.00 39.85 ATOM 3252 C TYR B 833 1.616 9.253 −32.734 1.00 41.61 ATOM 3253 O TYR B 833 0.714 9.143 −33.572 1.00 39.17 ATOM 3254 CB TYR B 833 2.048 11.521 −31.824 1.00 39.98 ATOM 3255 CG TYR B 833 1.369 12.250 −32.970 1.00 42.77 ATOM 3256 CD1 TYR B 833 0.311 13.147 −32.737 1.00 41.95 ATOM 3257 CD2 TYR B 833 1.787 12.053 −34.290 1.00 38.99 ATOM 3258 CE1 TYR B 833 −0.301 13.832 −33.798 1.00 38.79 ATOM 3259 CE2 TYR B 833 1.184 12.724 −35.345 1.00 38.68 ATOM 3260 CZ TYR B 833 0.145 13.612 −35.097 1.00 40.21 ATOM 3261 OH TYR B 833 −0.433 14.279 −36.159 1.00 40.82 ATOM 3262 N LEU B 834 2.784 8.619 −32.829 1.00 42.19 ATOM 3263 CA LEU B 834 3.080 7.721 −33.944 1.00 43.73 ATOM 3264 C LEU B 834 2.265 6.423 −33.844 1.00 44.01 ATOM 3265 O LEU B 834 1.736 5.937 −34.845 1.00 42.17 ATOM 3266 CB LEU B 834 4.584 7.384 −33.989 1.00 45.03 ATOM 3267 CG LEU B 834 5.669 8.440 −34.301 1.00 47.70 ATOM 3268 CD1 LEU B 834 7.028 7.851 −33.978 1.00 46.80 ATOM 3269 CD2 LEU B 834 5.649 8.858 −35.759 1.00 44.71 ATOM 3270 N GLU B 835 2.166 5.866 −32.640 1.00 44.61 ATOM 3271 CA GLU B 835 1.428 4.624 −32.444 1.00 48.10 ATOM 3272 C GLU B 835 −0.053 4.827 −32.708 1.00 50.02 ATOM 3273 O GLU B 835 −0.735 3.937 −33.215 1.00 48.65 ATOM 3274 CB GLU B 835 1.622 4.089 −31.027 1.00 48.14 ATOM 3275 CG GLU B 835 0.745 2.893 −30.733 1.00 51.80 ATOM 3276 CD GLU B 835 0.921 2.380 −29.327 1.00 55.96 ATOM 3277 OE1 GLU B 835 1.020 3.212 −28.401 1.00 58.77 ATOM 3278 OE2 GLU B 835 0.949 1.147 −29.139 1.00 59.79 ATOM 3279 N GLU B 836 −0.537 6.008 −32.347 1.00 51.95 ATOM 3280 CA GLU B 836 −1.926 6.378 −32.545 1.00 53.09 ATOM 3281 C GLU B 836 −2.227 6.270 −34.048 1.00 52.44 ATOM 3282 O GLU B 836 −3.325 5.874 −34.442 1.00 52.73 ATOM 3283 CB GLU B 836 −2.121 7.807 −32.029 1.00 55.57 ATOM 3284 CG GLU B 836 −3.548 8.296 −31.901 1.00 62.73 ATOM 3285 CD GLU B 836 −3.630 9.684 −31.243 1.00 69.86 ATOM 3286 OE1 GLU B 836 −4.721 10.308 −31.286 1.00 71.77 ATOM 3287 OE2 GLU B 836 −2.606 10.150 −30.677 1.00 71.84 ATOM 3288 N ARG B 837 −1.233 6.597 −34.875 1.00 50.86 ATOM 3289 CA ARG B 837 −1.361 6.550 −36.339 1.00 51.45 ATOM 3290 C ARG B 837 −0.926 5.206 −36.939 1.00 50.30 ATOM 3291 O ARG B 837 −0.750 5.098 −38.148 1.00 47.12 ATOM 3292 CB ARG B 837 −0.501 7.650 −36.987 1.00 53.02 ATOM 3293 CG ARG B 837 −0.781 9.066 −36.521 1.00 55.22 ATOM 3294 CD ARG B 837 −2.239 9.377 −36.704 1.00 58.03 ATOM 3295 NE ARG B 837 −2.603 10.765 −36.431 1.00 59.91 ATOM 3296 CZ ARG B 837 −2.371 11.412 −35.294 1.00 58.31 ATOM 3297 NH1 ARG B 837 −1.745 10.822 −34.282 1.00 57.92 ATOM 3298 NH2 ARG B 837 −2.830 12.645 −35.152 1.00 57.89 ATOM 3299 N ARG B 838 −0.754 4.198 −36.086 1.00 51.66 ATOM 3300 CA ARG B 838 −0.295 2.864 −36.489 1.00 51.85 ATOM 3301 C ARG B 838 1.055 2.920 −37.202 1.00 49.65 ATOM 3302 O ARG B 838 1.290 2.213 −38.186 1.00 50.29 ATOM 3303 CB ARG B 838 −1.334 2.143 −37.369 1.00 53.63 ATOM 3304 CG ARG B 838 −2.470 1.492 −36.575 1.00 59.68 ATOM 3305 CD ARG B 838 −1.932 0.532 −35.496 1.00 64.00 ATOM 3306 NE ARG B 838 −1.885 −0.866 −35.933 1.00 69.82 ATOM 3307 CZ ARG B 838 −2.913 −1.717 −35.876 1.00 71.87 ATOM 3308 NH1 ARG B 838 −2.764 −2.966 −36.307 1.00 71.46 ATOM 3309 NH2 ARG B 838 −4.084 −1.332 −35.374 1.00 72.32 ATOM 3310 N LEU B 839 1.945 3.759 −36.692 1.00 45.08 ATOM 3311 CA LEU B 839 3.263 3.886 −37.282 1.00 44.44 ATOM 3312 C LEU B 839 4.350 3.426 −36.319 1.00 44.15 ATOM 3313 O LEU B 839 4.454 3.900 −35.183 1.00 43.92 ATOM 3314 CB LEU B 839 3.512 5.331 −37.699 1.00 45.11 ATOM 3315 CG LEU B 839 2.429 5.939 −38.601 1.00 47.37 ATOM 3316 CD1 LEU B 839 2.763 7.407 −38.852 1.00 45.99 ATOM 3317 CD2 LEU B 839 2.317 5.161 −39.921 1.00 43.39 ATOM 3318 N VAL B 840 5.152 2.481 −36.785 1.00 43.12 ATOM 3319 CA VAL B 840 6.246 1.936 −36.000 1.00 42.97 ATOM 3320 C VAL B 840 7.543 2.589 −36.490 1.00 43.65 ATOM 3321 O VAL B 840 7.796 2.628 −37.690 1.00 44.79 ATOM 3322 CB VAL B 840 6.305 0.408 −36.192 1.00 42.39 ATOM 3323 CG1 VAL B 840 7.382 −0.221 −35.307 1.00 42.09 ATOM 3324 CG2 VAL B 840 4.945 −0.177 −35.881 1.00 41.99 ATOM 3325 N HIS B 841 8.351 3.110 −35.570 1.00 43.05 ATOM 3326 CA HIS B 841 9.613 3.756 −35.932 1.00 43.35 ATOM 3327 C HIS B 841 10.680 2.760 −36.412 1.00 44.72 ATOM 3328 O HIS B 841 11.258 2.927 −37.485 1.00 45.10 ATOM 3329 CB HIS B 841 10.150 4.547 −34.736 1.00 41.90 ATOM 3330 CG HIS B 841 11.221 5.535 −35.090 1.00 40.88 ATOM 3331 ND1 HIS B 841 12.406 5.170 −35.690 1.00 39.11 ATOM 3332 CD2 HIS B 841 11.289 6.876 −34.917 1.00 41.53 ATOM 3333 CE1 HIS B 841 13.156 6.242 −35.870 1.00 40.04 ATOM 3334 NE2 HIS B 841 12.502 7.291 −35.409 1.00 39.97 ATOM 3335 N ARG B 842 10.937 1.731 −35.607 1.00 46.60 ATOM 3336 CA ARG B 842 11.927 0.691 −35.915 1.00 47.69 ATOM 3337 C ARG B 842 13.380 1.106 −35.704 1.00 47.11 ATOM 3338 O ARG B 842 14.260 0.250 −35.650 1.00 47.21 ATOM 3339 CB ARG B 842 11.794 0.199 −37.356 1.00 48.94 ATOM 3340 CG ARG B 842 10.483 −0.442 −37.701 1.00 53.39 ATOM 3341 CD ARG B 842 10.558 −1.004 −39.106 1.00 56.65 ATOM 3342 NE ARG B 842 9.354 −1.720 −39.505 1.00 57.96 ATOM 3343 CZ ARG B 842 9.326 −2.590 −40.504 1.00 59.81 ATOM 3344 NH1 ARG B 842 10.435 −2.834 −41.183 1.00 61.66 ATOM 3345 NH2 ARG B 842 8.203 −3.216 −40.821 1.00 61.73 ATOM 3346 N ASP B 843 13.639 2.403 −35.587 1.00 45.43 ATOM 3347 CA ASP B 843 15.009 2.862 −35.402 1.00 44.93 ATOM 3348 C ASP B 843 15.108 4.035 −34.427 1.00 43.50 ATOM 3349 O ASP B 843 15.803 5.029 −34.679 1.00 40.29 ATOM 3350 CB ASP B 843 15.602 3.234 −36.769 1.00 48.21 ATOM 3351 CG ASP B 843 17.058 3.636 −36.687 1.00 49.17 ATOM 3352 OD1 ASP B 843 17.829 2.925 −36.005 1.00 50.67 ATOM 3353 OD2 ASP B 843 17.424 4.656 −37.309 1.00 50.03 ATOM 3354 N LEU B 844 14.397 3.914 −33.312 1.00 41.09 ATOM 3355 CA LEU B 844 14.409 4.942 −32.296 1.00 39.45 ATOM 3356 C LEU B 844 15.683 4.757 −31.476 1.00 41.41 ATOM 3357 O LEU B 844 15.962 3.662 −30.982 1.00 39.94 ATOM 3358 CB LEU B 844 13.192 4.802 −31.394 1.00 37.57 ATOM 3359 CG LEU B 844 13.136 5.718 −30.161 1.00 37.58 ATOM 3360 CD1 LEU B 844 12.897 7.175 −30.572 1.00 31.85 ATOM 3361 CD2 LEU B 844 12.023 5.232 −29.248 1.00 33.61 ATOM 3362 N ALA B 845 16.461 5.825 −31.356 1.00 41.14 ATOM 3363 CA ALA B 845 17.703 5.793 −30.594 1.00 43.80 ATOM 3364 C ALA B 845 17.998 7.233 −30.239 1.00 44.77 ATOM 3365 O ALA B 845 17.463 8.139 −30.872 1.00 46.46 ATOM 3366 CB ALA B 845 18.839 5.208 −31.436 1.00 43.20 ATOM 3367 N ALA B 846 18.838 7.462 −29.241 1.00 44.58 ATOM 3368 CA ALA B 846 19.124 8.833 −28.856 1.00 45.24 ATOM 3369 C ALA B 846 19.609 9.661 −30.030 1.00 45.63 ATOM 3370 O ALA B 846 19.289 10.850 −30.115 1.00 47.93 ATOM 3371 CB ALA B 846 20.142 8.870 −27.734 1.00 45.17 ATOM 3372 N ARG B 847 20.363 9.045 −30.941 1.00 44.22 ATOM 3373 CA ARG B 847 20.886 9.786 −32.094 1.00 46.27 ATOM 3374 C ARG B 847 19.800 10.270 −33.054 1.00 46.18 ATOM 3375 O ARG B 847 20.043 11.161 −33.865 1.00 46.55 ATOM 3376 CB ARG B 847 21.895 8.951 −32.877 1.00 46.11 ATOM 3377 CG ARG B 847 21.254 7.928 −33.760 1.00 49.88 ATOM 3378 CD ARG B 847 22.263 7.195 −34.602 1.00 50.73 ATOM 3379 NE ARG B 847 21.564 6.353 −35.565 1.00 57.37 ATOM 3380 CZ ARG B 847 20.873 5.264 −35.242 1.00 58.79 ATOM 3381 NH1 ARG B 847 20.794 4.872 −33.976 1.00 60.01 ATOM 3382 NH2 ARG B 847 20.243 4.576 −36.182 1.00 59.64 ATOM 3383 N ASN B 848 18.610 9.683 −32.978 1.00 45.11 ATOM 3384 CA ASN B 848 17.532 10.114 −33.848 1.00 45.22 ATOM 3385 C ASN B 848 16.525 11.015 −33.132 1.00 47.16 ATOM 3386 O ASN B 848 15.351 11.117 −33.525 1.00 46.11 ATOM 3387 CB ASN B 848 16.840 8.917 −34.500 1.00 43.37 ATOM 3388 CG ASN B 848 17.576 8.434 −35.736 1.00 44.82 ATOM 3389 OD1 ASN B 848 17.953 9.234 −36.596 1.00 47.01 ATOM 3390 ND2 ASN B 848 17.781 7.127 −35.838 1.00 42.89 ATOM 3391 N VAL B 849 16.996 11.657 −32.065 1.00 47.02 ATOM 3392 CA VAL B 849 16.181 12.606 −31.330 1.00 48.04 ATOM 3393 C VAL B 849 16.951 13.914 −31.472 1.00 48.97 ATOM 3394 O VAL B 849 18.134 13.987 −31.146 1.00 49.90 ATOM 3395 CB VAL B 849 16.026 12.235 −29.829 1.00 48.21 ATOM 3396 CG1 VAL B 849 15.223 13.322 −29.109 1.00 48.81 ATOM 3397 CG2 VAL B 849 15.298 10.899 −29.689 1.00 46.65 ATOM 3398 N LEU B 850 16.281 14.934 −31.995 1.00 50.30 ATOM 3399 CA LEU B 850 16.900 16.234 −32.216 1.00 49.70 ATOM 3400 C LEU B 850 16.503 17.241 −31.144 1.00 51.97 ATOM 3401 O LEU B 850 15.449 17.116 −30.514 1.00 53.21 ATOM 3402 CB LEU B 850 16.490 16.768 −33.583 1.00 46.49 ATOM 3403 CG LEU B 850 16.660 15.825 −34.771 1.00 45.29 ATOM 3404 CD1 LEU B 850 16.076 16.481 −35.999 1.00 43.36 ATOM 3405 CD2 LEU B 850 18.120 15.500 −34.986 1.00 44.40 ATOM 3406 N VAL B 851 17.352 18.249 −30.954 1.00 53.33 ATOM 3407 CA VAL B 851 17.112 19.284 −29.960 1.00 53.66 ATOM 3408 C VAL B 851 16.731 20.610 −30.628 1.00 55.93 ATOM 3409 O VAL B 851 17.595 21.317 −31.153 1.00 56.57 ATOM 3410 CB VAL B 851 18.375 19.494 −29.094 1.00 52.04 ATOM 3411 CG1 VAL B 851 18.081 20.455 −27.966 1.00 53.25 ATOM 3412 CG2 VAL B 851 18.850 18.171 −28.540 1.00 50.16 ATOM 3413 N LYS B 852 15.440 20.940 −30.624 1.00 57.66 ATOM 3414 CA LYS B 852 14.982 22.196 −31.222 1.00 60.00 ATOM 3415 C LYS B 852 15.497 23.295 −30.317 1.00 62.13 ATOM 3416 O LYS B 852 15.977 24.328 −30.778 1.00 64.39 ATOM 3417 CB LYS B 852 13.458 22.268 −31.272 1.00 58.87 ATOM 3418 CG LYS B 852 12.923 23.615 −31.741 1.00 58.96 ATOM 3419 CD LYS B 852 11.398 23.646 −31.691 1.00 60.41 ATOM 3420 CE LYS B 852 10.817 24.892 −32.352 1.00 60.45 ATOM 3421 NZ LYS B 852 9.312 24.862 −32.407 1.00 61.83 ATOM 3422 N SER B 853 15.374 23.050 −29.017 1.00 61.87 ATOM 3423 CA SER B 853 15.837 23.960 −27.980 1.00 61.38 ATOM 3424 C SER B 853 15.945 23.145 −26.680 1.00 61.16 ATOM 3425 O SER B 853 15.236 22.157 −26.489 1.00 58.97 ATOM 3426 CB SER B 853 14.878 25.147 −27.822 1.00 59.92 ATOM 3427 OG SER B 853 13.582 24.731 −27.445 1.00 61.79 ATOM 3428 N PRO B 854 16.851 23.546 −25.780 1.00 61.17 ATOM 3429 CA PRO B 854 17.076 22.865 −24.503 1.00 60.56 ATOM 3430 C PRO B 854 15.876 22.143 −23.892 1.00 59.89 ATOM 3431 O PRO B 854 15.957 20.959 −23.555 1.00 59.58 ATOM 3432 CB PRO B 854 17.599 23.986 −23.625 1.00 61.16 ATOM 3433 CG PRO B 854 18.478 24.738 −24.599 1.00 62.45 ATOM 3434 CD PRO B 854 17.600 24.818 −25.834 1.00 62.08 ATOM 3435 N ALA B 855 14.764 22.850 −23.762 1.00 57.36 ATOM 3436 CA ALA B 855 13.576 22.269 −23.173 1.00 55.01 ATOM 3437 C ALA B 855 12.621 21.699 −24.210 1.00 55.18 ATOM 3438 O ALA B 855 11.440 21.533 −23.929 1.00 54.40 ATOM 3439 CB ALA B 855 12.867 23.323 −22.354 1.00 54.10 ATOM 3440 N HIS B 856 13.116 21.368 −25.399 1.00 55.23 ATOM 3441 CA HIS B 856 12.222 20.881 −26.448 1.00 52.68 ATOM 3442 C HIS B 856 12.891 19.970 −27.478 1.00 51.26 ATOM 3443 O HIS B 856 13.649 20.427 −28.343 1.00 51.11 ATOM 3444 CB HIS B 856 11.602 22.096 −27.148 1.00 53.04 ATOM 3445 CG HIS B 856 10.492 21.766 −28.097 1.00 55.71 ATOM 3446 ND1 HIS B 856 9.868 22.714 −28.880 1.00 55.62 ATOM 3447 CD2 HIS B 856 9.902 20.583 −28.396 1.00 54.97 ATOM 3448 CE1 HIS B 856 8.943 22.129 −29.619 1.00 55.10 ATOM 3449 NE2 HIS B 856 8.942 20.837 −29.344 1.00 55.98 ATOM 3450 N VAL B 857 12.602 18.677 −27.388 1.00 48.98 ATOM 3451 CA VAL B 857 13.164 17.717 −28.328 1.00 47.33 ATOM 3452 C VAL B 857 12.076 17.225 −29.291 1.00 46.32 ATOM 3453 O VAL B 857 10.877 17.362 −29.018 1.00 45.36 ATOM 3454 CB VAL B 857 13.827 16.500 −27.593 1.00 46.33 ATOM 3455 CG1 VAL B 857 15.094 16.944 −26.897 1.00 44.86 ATOM 3456 CG2 VAL B 857 12.874 15.902 −26.581 1.00 44.39 ATOM 3457 N LYS B 858 12.516 16.681 −30.425 1.00 44.31 ATOM 3458 CA LYS B 858 11.636 16.145 −31.459 1.00 43.59 ATOM 3459 C LYS B 858 12.222 14.849 −32.014 1.00 43.20 ATOM 3460 O LYS B 858 13.438 14.753 −32.217 1.00 43.70 ATOM 3461 CB LYS B 858 11.492 17.140 −32.614 1.00 44.67 ATOM 3462 CG LYS B 858 10.538 18.301 −32.362 1.00 46.35 ATOM 3463 CD LYS B 858 10.463 19.170 −33.610 1.00 46.33 ATOM 3464 CE LYS B 858 9.382 20.215 −33.508 1.00 46.98 ATOM 3465 NZ LYS B 858 9.214 20.892 −34.816 1.00 50.99 ATOM 3466 N ILE B 859 11.367 13.855 −32.265 1.00 42.00 ATOM 3467 CA ILE B 859 11.832 12.583 −32.816 1.00 39.14 ATOM 3468 C ILE B 859 11.955 12.719 −34.328 1.00 39.96 ATOM 3469 O ILE B 859 11.140 13.386 −34.966 1.00 40.22 ATOM 3470 CB ILE B 859 10.863 11.431 −32.480 1.00 37.12 ATOM 3471 CG1 ILE B 859 10.738 11.297 −30.958 1.00 37.67 ATOM 3472 CG2 ILE B 859 11.384 10.129 −33.069 1.00 34.33 ATOM 3473 CD1 ILE B 859 9.834 10.171 −30.480 1.00 33.72 ATOM 3474 N THR B 860 12.977 12.093 −34.900 1.00 41.18 ATOM 3475 CA THR B 860 13.197 12.174 −36.342 1.00 43.70 ATOM 3476 C THR B 860 13.596 10.844 −36.971 1.00 45.83 ATOM 3477 O THR B 860 14.019 9.918 −36.278 1.00 47.50 ATOM 3478 CB THR B 860 14.312 13.218 −36.688 1.00 42.70 ATOM 3479 OG1 THR B 860 14.311 13.486 −38.096 1.00 41.02 ATOM 3480 CG2 THR B 860 15.685 12.683 −36.317 1.00 41.73 ATOM 3481 N ASP B 861 13.463 10.772 −38.294 1.00 46.92 ATOM 3482 CA ASP B 861 13.839 9.597 −39.078 1.00 49.85 ATOM 3483 C ASP B 861 12.873 8.419 −39.058 1.00 50.50 ATOM 3484 O ASP B 861 13.233 7.317 −39.458 1.00 50.83 ATOM 3485 CB ASP B 861 15.239 9.109 −38.680 1.00 50.52 ATOM 3486 CG ASP B 861 16.070 8.688 −39.883 1.00 54.77 ATOM 3487 OD1 ASP B 861 16.304 9.533 −40.764 1.00 56.69 ATOM 3488 OD2 ASP B 861 16.495 7.518 −39.959 1.00 58.38 ATOM 3489 N PHE B 862 11.649 8.633 −38.600 1.00 52.16 ATOM 3490 CA PHE B 862 10.689 7.542 −38.606 1.00 55.68 ATOM 3491 C PHE B 862 10.256 7.323 −40.057 1.00 58.32 ATOM 3492 O PHE B 862 10.120 8.281 −40.823 1.00 59.56 ATOM 3493 CB PHE B 862 9.472 7.873 −37.732 1.00 55.12 ATOM 3494 CG PHE B 862 8.874 9.233 −37.995 1.00 54.59 ATOM 3495 CD1 PHE B 862 9.153 10.303 −37.149 1.00 54.37 ATOM 3496 CD2 PHE B 862 8.038 9.445 −39.085 1.00 53.46 ATOM 3497 CE1 PHE B 862 8.610 11.560 −37.385 1.00 53.72 ATOM 3498 CE2 PHE B 862 7.489 10.700 −39.331 1.00 52.07 ATOM 3499 CZ PHE B 862 7.777 11.757 −38.478 1.00 53.20 ATOM 3500 N GLY B 863 10.066 6.068 −40.446 1.00 60.33 ATOM 3501 CA GLY B 863 9.646 5.797 −41.809 1.00 64.81 ATOM 3502 C GLY B 863 10.679 5.163 −42.725 1.00 68.14 ATOM 3503 O GLY B 863 10.377 4.174 −43.393 1.00 68.10 ATOM 3504 N LEU B 864 11.887 5.726 −42.768 1.00 70.85 ATOM 3505 CA LEU B 864 12.952 5.194 −43.622 1.00 73.25 ATOM 3506 C LEU B 864 13.219 3.714 −43.386 1.00 74.47 ATOM 3507 O LEU B 864 13.373 2.950 −44.335 1.00 76.25 ATOM 3508 CB LEU B 864 14.267 5.949 −43.412 1.00 73.37 ATOM 3509 CG LEU B 864 14.399 7.414 −43.815 1.00 72.75 ATOM 3510 CD1 LEU B 864 15.853 7.800 −43.685 1.00 72.55 ATOM 3511 CD2 LEU B 864 13.925 7.633 −45.237 1.00 72.97 ATOM 3512 N ALA B 865 13.291 3.319 −42.121 1.00 74.99 ATOM 3513 CA ALA B 865 13.549 1.932 −41.769 1.00 75.61 ATOM 3514 C ALA B 865 12.791 0.967 −42.679 1.00 76.21 ATOM 3515 O ALA B 865 13.392 0.215 −43.456 1.00 76.63 ATOM 3516 CB ALA B 865 13.163 1.692 −40.322 1.00 76.18 ATOM 3517 N ARG B 866 11.467 1.001 −42.582 1.00 75.63 ATOM 3518 CA ARG B 866 10.615 0.127 −43.377 1.00 74.69 ATOM 3519 C ARG B 866 10.806 0.377 −44.866 1.00 72.85 ATOM 3520 O ARG B 866 10.788 −0.555 −45.672 1.00 72.17 ATOM 3521 CB ARG B 866 9.150 0.355 −43.010 1.00 77.16 ATOM 3522 CG ARG B 866 8.192 −0.678 −43.579 1.00 80.89 ATOM 3523 CD ARG B 866 6.766 −0.351 −43.162 1.00 84.67 ATOM 3524 NE ARG B 866 5.889 −1.518 −43.176 1.00 87.14 ATOM 3525 CZ ARG B 866 4.665 −1.535 −42.656 1.00 89.52 ATOM 3526 NH1 ARG B 866 4.169 −0.441 −42.081 1.00 89.56 ATOM 3527 NH2 ARG B 866 3.942 −2.648 −42.698 1.00 90.37 ATOM 3528 N LEU B 867 10.999 1.639 −45.229 1.00 69.43 ATOM 3529 CA LEU B 867 11.173 1.993 −46.630 1.00 68.73 ATOM 3530 C LEU B 867 12.416 1.394 −47.275 1.00 68.30 ATOM 3531 O LEU B 867 12.376 0.980 −48.433 1.00 68.60 ATOM 3532 CB LEU B 867 11.206 3.513 −46.801 1.00 67.15 ATOM 3533 CG LEU B 867 11.287 3.964 −48.258 1.00 63.74 ATOM 3534 CD1 LEU B 867 10.063 3.458 −49.008 1.00 62.81 ATOM 3535 CD2 LEU B 867 11.384 5.474 −48.331 1.00 61.46 ATOM 3536 N LEU B 868 13.516 1.348 −46.532 1.00 67.70 ATOM 3537 CA LEU B 868 14.759 0.810 −47.066 1.00 67.56 ATOM 3538 C LEU B 868 14.851 −0.703 −46.951 1.00 66.73 ATOM 3539 O LEU B 868 15.386 −1.361 −47.841 1.00 65.40 ATOM 3540 CB LEU B 868 15.963 1.446 −46.365 1.00 69.33 ATOM 3541 CG LEU B 868 15.984 2.976 −46.258 1.00 71.54 ATOM 3542 CD1 LEU B 868 17.337 3.418 −45.705 1.00 71.31 ATOM 3543 CD2 LEU B 868 15.719 3.613 −47.617 1.00 70.98 ATOM 3544 N GLU B 869 14.329 −1.263 −45.865 1.00 66.47 ATOM 3545 CA GLU B 869 14.393 −2.705 −45.692 1.00 66.24 ATOM 3546 C GLU B 869 13.191 −3.433 −46.271 1.00 65.56 ATOM 3547 O GLU B 869 13.276 −4.020 −47.345 1.00 66.35 ATOM 3548 CB GLU B 869 14.547 −3.055 −44.220 1.00 67.33 ATOM 3549 CG GLU B 869 15.784 −2.462 −43.592 1.00 69.61 ATOM 3550 CD GLU B 869 16.423 −3.390 −42.579 1.00 71.71 ATOM 3551 OE1 GLU B 869 15.728 −3.811 −41.620 1.00 70.66 ATOM 3552 OE2 GLU B 869 17.625 −3.697 −42.752 1.00 72.27 ATOM 3553 N GLY B 870 12.073 −3.396 −45.563 1.00 64.97 ATOM 3554 CA GLY B 870 10.888 −4.076 −46.041 1.00 64.73 ATOM 3555 C GLY B 870 10.238 −4.819 −44.900 1.00 65.26 ATOM 3556 O GLY B 870 10.555 −4.567 −43.744 1.00 64.41 ATOM 3557 N ASP B 871 9.344 −5.748 −45.216 1.00 66.68 ATOM 3558 CA ASP B 871 8.647 −6.501 −44.182 1.00 67.47 ATOM 3559 C ASP B 871 8.975 −7.982 −44.162 1.00 66.00 ATOM 3560 O ASP B 871 8.345 −8.747 −43.434 1.00 65.97 ATOM 3561 CB ASP B 871 7.137 −6.327 −44.351 1.00 72.20 ATOM 3562 CG ASP B 871 6.676 −4.927 −44.013 1.00 76.99 ATOM 3563 OD1 ASP B 871 6.783 −4.551 −42.824 1.00 80.07 ATOM 3564 OD2 ASP B 871 6.216 −4.204 −44.930 1.00 78.50 ATOM 3565 N GLU B 872 9.961 −8.389 −44.951 1.00 64.83 ATOM 3566 CA GLU B 872 10.333 −9.794 −45.018 1.00 63.94 ATOM 3567 C GLU B 872 10.666 −10.338 −43.631 1.00 61.57 ATOM 3568 O GLU B 872 11.580 −9.857 −42.963 1.00 60.56 ATOM 3569 CB GLU B 872 11.522 −9.969 −45.961 1.00 66.69 ATOM 3570 CG GLU B 872 11.932 −11.418 −46.172 1.00 71.91 ATOM 3571 CD GLU B 872 13.047 −11.569 −47.202 1.00 76.05 ATOM 3572 OE1 GLU B 872 13.408 −10.553 −47.842 1.00 76.98 ATOM 3573 OE2 GLU B 872 13.557 −12.702 −47.378 1.00 77.59 ATOM 3574 N ALA B 873 9.914 −11.342 −43.202 1.00 59.27 ATOM 3575 CA ALA B 873 10.124 −11.935 −41.894 1.00 57.77 ATOM 3576 C ALA B 873 11.549 −12.447 −41.719 1.00 58.33 ATOM 3577 O ALA B 873 12.171 −12.267 −40.668 1.00 56.59 ATOM 3578 CB ALA B 873 9.133 −13.070 −41.679 1.00 55.37 ATOM 3579 N ALA B 874 12.076 −13.086 −42.755 1.00 59.61 ATOM 3580 CA ALA B 874 13.418 −13.640 −42.666 1.00 60.12 ATOM 3581 C ALA B 874 14.500 −12.681 −43.134 1.00 60.09 ATOM 3582 O ALA B 874 14.395 −12.075 −44.203 1.00 60.48 ATOM 3583 CB ALA B 874 13.494 −14.949 −43.456 1.00 59.26 ATOM 3584 N TYR B 875 15.538 −12.542 −42.316 1.00 59.00 ATOM 3585 CA TYR B 875 16.667 −11.688 −42.655 1.00 58.29 ATOM 3586 C TYR B 875 17.575 −12.464 −43.595 1.00 58.10 ATOM 3587 O TYR B 875 17.824 −13.649 −43.388 1.00 57.86 ATOM 3588 CB TYR B 875 17.487 −11.336 −41.414 1.00 58.23 ATOM 3589 CG TYR B 875 16.842 −10.360 −40.466 1.00 58.80 ATOM 3590 CD1 TYR B 875 16.632 −9.033 −40.842 1.00 57.46 ATOM 3591 CD2 TYR B 875 16.456 −10.759 −39.185 1.00 56.30 ATOM 3592 CE1 TYR B 875 16.056 −8.126 −39.970 1.00 58.87 ATOM 3593 CE2 TYR B 875 15.879 −9.862 −38.303 1.00 59.49 ATOM 3594 CZ TYR B 875 15.680 −8.543 −38.701 1.00 60.51 ATOM 3595 OH TYR B 875 15.102 −7.645 −37.834 1.00 60.20 ATOM 3596 N ASN B 876 18.060 −11.802 −44.634 1.00 58.32 ATOM 3597 CA ASN B 876 18.984 −12.440 −45.550 1.00 58.92 ATOM 3598 C ASN B 876 20.368 −12.237 −44.912 1.00 59.09 ATOM 3599 O ASN B 876 20.457 −11.766 −43.775 1.00 57.47 ATOM 3600 CB ASN B 876 18.879 −11.805 −46.943 1.00 59.97 ATOM 3601 CG ASN B 876 18.810 −10.286 −46.903 1.00 65.32 ATOM 3602 OD1 ASN B 876 18.123 −9.696 −46.055 1.00 69.32 ATOM 3603 ND2 ASN B 876 19.505 −9.638 −47.836 1.00 65.71 ATOM 3604 N ALA B 877 21.435 −12.596 −45.617 1.00 59.32 ATOM 3605 CA ALA B 877 22.787 −12.466 −45.077 1.00 59.77 ATOM 3606 C ALA B 877 23.238 −11.011 −44.883 1.00 61.45 ATOM 3607 O ALA B 877 24.270 −10.746 −44.245 1.00 59.71 ATOM 3608 CB ALA B 877 23.765 −13.201 −45.983 1.00 60.47 ATOM 3609 N ASP B 878 22.459 −10.079 −45.434 1.00 62.48 ATOM 3610 CA ASP B 878 22.753 −8.654 −45.334 1.00 62.92 ATOM 3611 C ASP B 878 22.260 −8.132 −43.987 1.00 63.34 ATOM 3612 O ASP B 878 22.660 −7.055 −43.548 1.00 63.62 ATOM 3613 CB ASP B 878 22.067 −7.894 −46.479 1.00 62.83 ATOM 3614 CG ASP B 878 22.688 −6.519 −46.737 1.00 64.73 ATOM 3615 OD1 ASP B 878 23.921 −6.442 −46.947 1.00 63.55 ATOM 3616 OD2 ASP B 878 21.938 −5.516 −46.745 1.00 64.59 ATOM 3617 N GLY B 879 21.386 −8.902 −43.340 1.00 63.87 ATOM 3618 CA GLY B 879 20.847 −8.516 −42.042 1.00 65.56 ATOM 3619 C GLY B 879 19.955 −7.281 −42.027 1.00 65.90 ATOM 3620 O GLY B 879 19.336 −6.933 −43.037 1.00 66.17 ATOM 3621 N GLY B 880 19.885 −6.621 −40.873 1.00 65.12 ATOM 3622 CA GLY B 880 19.074 −5.422 −40.754 1.00 64.82 ATOM 3623 C GLY B 880 19.899 −4.157 −40.938 1.00 64.56 ATOM 3624 O GLY B 880 21.107 −4.229 −41.141 1.00 64.99 ATOM 3625 N ALA B 881 19.259 −2.995 −40.871 1.00 63.83 ATOM 3626 CA ALA B 881 19.978 −1.736 −41.025 1.00 63.13 ATOM 3627 C ALA B 881 20.131 −1.016 −39.686 1.00 62.11 ATOM 3628 O ALA B 881 21.023 −0.188 −39.522 1.00 61.84 ATOM 3629 CB ALA B 881 19.261 −0.835 −42.033 1.00 63.27 ATOM 3630 N MET B 882 19.270 −1.334 −38.726 1.00 60.73 ATOM 3631 CA MET B 882 19.346 −0.692 −37.422 1.00 60.66 ATOM 3632 C MET B 882 20.388 −1.349 −36.543 1.00 57.66 ATOM 3633 O MET B 882 20.738 −2.505 −36.742 1.00 58.53 ATOM 3634 CB MET B 882 18.006 −0.759 −36.692 1.00 64.90 ATOM 3635 CG MET B 882 16.844 −0.168 −37.442 1.00 71.12 ATOM 3636 SD MET B 882 16.275 −1.292 −38.702 1.00 79.62 ATOM 3637 CE MET B 882 16.473 −0.256 −40.127 1.00 78.23 ATOM 3638 N PRO B 883 20.906 −0.610 −35.558 1.00 54.95 ATOM 3639 CA PRO B 883 21.910 −1.186 −34.666 1.00 54.93 ATOM 3640 C PRO B 883 21.262 −2.267 −33.804 1.00 54.49 ATOM 3641 O PRO B 883 20.201 −2.054 −33.239 1.00 55.33 ATOM 3642 CB PRO B 883 22.392 0.022 −33.869 1.00 54.23 ATOM 3643 CG PRO B 883 21.206 0.944 −33.882 1.00 55.31 ATOM 3644 CD PRO B 883 20.719 0.826 −35.291 1.00 53.61 ATOM 3645 N ILE B 884 21.904 −3.427 −33.710 1.00 55.18 ATOM 3646 CA ILE B 884 21.363 −4.549 −32.949 1.00 54.75 ATOM 3647 C ILE B 884 21.109 −4.230 −31.481 1.00 53.77 ATOM 3648 O ILE B 884 20.193 −4.778 −30.871 1.00 52.49 ATOM 3649 CB ILE B 884 22.315 −5.786 −32.997 1.00 57.45 ATOM 3650 CG1 ILE B 884 22.977 −5.911 −34.379 1.00 60.74 ATOM 3651 CG2 ILE B 884 21.522 −7.070 −32.704 1.00 56.49 ATOM 3652 CD1 ILE B 884 22.026 −6.282 −35.528 1.00 61.29 ATOM 3653 N LYS B 885 21.912 −3.333 −30.919 1.00 53.13 ATOM 3654 CA LYS B 885 21.809 −3.004 −29.499 1.00 51.92 ATOM 3655 C LYS B 885 20.604 −2.183 −29.040 1.00 50.73 ATOM 3656 O LYS B 885 20.309 −2.099 −27.850 1.00 50.67 ATOM 3657 CB LYS B 885 23.118 −2.350 −29.052 1.00 51.96 ATOM 3658 CG LYS B 885 24.316 −3.277 −29.214 1.00 49.00 ATOM 3659 CD LYS B 885 25.597 −2.616 −28.766 1.00 52.24 ATOM 3660 CE LYS B 885 26.798 −3.482 −29.122 1.00 53.83 ATOM 3661 NZ LYS B 885 28.091 −2.784 −28.862 1.00 56.01 ATOM 3662 N TRP B 886 19.900 −1.588 −29.985 1.00 48.96 ATOM 3663 CA TRP B 886 18.728 −0.797 −29.667 1.00 47.71 ATOM 3664 C TRP B 886 17.494 −1.600 −30.055 1.00 48.21 ATOM 3665 O TRP B 886 16.363 −1.142 −29.899 1.00 49.83 ATOM 3666 CB TRP B 886 18.765 0.501 −30.470 1.00 46.30 ATOM 3667 CG TRP B 886 19.594 1.587 −29.863 1.00 46.96 ATOM 3668 CD1 TRP B 886 19.138 2.657 −29.145 1.00 45.46 ATOM 3669 CD2 TRP B 886 21.014 1.750 −29.965 1.00 47.38 ATOM 3670 NE1 TRP B 886 20.182 3.480 −28.802 1.00 45.52 ATOM 3671 CE2 TRP B 886 21.346 2.950 −29.293 1.00 46.37 ATOM 3672 CE3 TRP B 886 22.039 1.003 −30.560 1.00 48.54 ATOM 3673 CZ2 TRP B 886 22.661 3.422 −29.202 1.00 44.45 ATOM 3674 CZ3 TRP B 886 23.354 1.479 −30.468 1.00 48.55 ATOM 3675 CH2 TRP B 886 23.648 2.678 −29.793 1.00 43.97 ATOM 3676 N MET B 887 17.731 −2.814 −30.536 1.00 47.39 ATOM 3677 CA MET B 887 16.689 −3.702 −31.038 1.00 47.29 ATOM 3678 C MET B 887 16.042 −4.632 −30.021 1.00 46.15 ATOM 3679 O MET B 887 16.716 −5.188 −29.170 1.00 44.83 ATOM 3680 CB MET B 887 17.299 −4.525 −32.182 1.00 49.51 ATOM 3681 CG MET B 887 16.366 −4.953 −33.287 1.00 52.27 ATOM 3682 SD MET B 887 17.296 −5.341 −34.809 1.00 53.59 ATOM 3683 CE MET B 887 17.031 −3.843 −35.775 1.00 56.07 ATOM 3684 N ALA B 888 14.723 −4.785 −30.119 1.00 48.05 ATOM 3685 CA ALA B 888 13.962 −5.683 −29.240 1.00 48.80 ATOM 3686 C ALA B 888 14.288 −7.110 −29.661 1.00 49.42 ATOM 3687 O ALA B 888 14.361 −7.406 −30.856 1.00 49.12 ATOM 3688 CB ALA B 888 12.460 −5.432 −29.386 1.00 47.59 ATOM 3689 N LEU B 889 14.472 −7.988 −28.681 1.00 50.17 ATOM 3690 CA LEU B 889 14.829 −9.376 −28.941 1.00 51.55 ATOM 3691 C LEU B 889 14.145 −10.030 −30.124 1.00 53.37 ATOM 3692 O LEU B 889 14.806 −10.463 −31.076 1.00 54.40 ATOM 3693 CB LEU B 889 14.570 −10.230 −27.713 1.00 52.02 ATOM 3694 CG LEU B 889 14.987 −11.690 −27.885 1.00 53.15 ATOM 3695 CD1 LEU B 889 16.443 −11.748 −28.320 1.00 52.50 ATOM 3696 CD2 LEU B 889 14.777 −12.445 −26.571 1.00 52.22 ATOM 3697 N GLU B 890 12.822 −10.114 −30.067 1.00 53.20 ATOM 3698 CA GLU B 890 12.079 −10.745 −31.146 1.00 54.27 ATOM 3699 C GLU B 890 12.498 −10.227 −32.521 1.00 55.82 ATOM 3700 O GLU B 890 12.562 −10.994 −33.480 1.00 57.28 ATOM 3701 CB GLU B 890 10.566 −10.557 −30.955 1.00 52.93 ATOM 3702 CG GLU B 890 10.094 −9.116 −31.001 1.00 50.27 ATOM 3703 CD GLU B 890 10.080 −8.445 −29.634 1.00 48.34 ATOM 3704 OE1 GLU B 890 10.893 −8.842 −28.759 1.00 44.27 ATOM 3705 OE2 GLU B 890 9.260 −7.509 −29.453 1.00 42.51 ATOM 3706 N CYS B 891 12.798 −8.935 −32.613 1.00 57.27 ATOM 3707 CA CYS B 891 13.192 −8.336 −33.888 1.00 58.36 ATOM 3708 C CYS B 891 14.617 −8.642 −34.313 1.00 58.40 ATOM 3709 O CYS B 891 15.052 −8.274 −35.401 1.00 56.71 ATOM 3710 CB CYS B 891 12.972 −6.826 −33.852 1.00 59.30 ATOM 3711 SG CYS B 891 11.232 −6.370 −33.986 1.00 58.60 ATOM 3712 N ILE B 892 15.352 −9.324 −33.457 1.00 59.69 ATOM 3713 CA ILE B 892 16.708 −9.677 −33.812 1.00 60.78 ATOM 3714 C ILE B 892 16.692 −10.959 −34.647 1.00 60.92 ATOM 3715 O ILE B 892 17.492 −11.104 −35.556 1.00 61.20 ATOM 3716 CB ILE B 892 17.584 −9.872 −32.549 1.00 60.34 ATOM 3717 CG1 ILE B 892 17.844 −8.516 −31.898 1.00 59.88 ATOM 3718 CG2 ILE B 892 18.892 −10.551 −32.910 1.00 58.41 ATOM 3719 CD1 ILE B 892 18.713 −8.585 −30.683 1.00 61.44 ATOM 3720 N HIS B 893 15.766 −11.873 −34.350 1.00 61.38 ATOM 3721 CA HIS B 893 15.676 −13.143 −35.071 1.00 60.14 ATOM 3722 C HIS B 893 14.811 −13.131 −36.329 1.00 57.92 ATOM 3723 O HIS B 893 15.010 −13.940 −37.232 1.00 56.94 ATOM 3724 CB HIS B 893 15.195 −14.245 −34.127 1.00 61.71 ATOM 3725 CG HIS B 893 16.205 −14.626 −33.092 1.00 65.26 ATOM 3726 ND1 HIS B 893 17.326 −15.375 −33.384 1.00 66.05 ATOM 3727 CD2 HIS B 893 16.239 −14.400 −31.756 1.00 65.76 ATOM 3728 CE1 HIS B 893 18.006 −15.596 −32.272 1.00 66.79 ATOM 3729 NE2 HIS B 893 17.368 −15.016 −31.270 1.00 67.66 ATOM 3730 N TYR B 894 13.850 −12.218 −36.379 1.00 55.44 ATOM 3731 CA TYR B 894 12.956 −12.082 −37.523 1.00 53.67 ATOM 3732 C TYR B 894 12.491 −10.649 −37.482 1.00 52.79 ATOM 3733 O TYR B 894 12.909 −9.893 −36.620 1.00 53.67 ATOM 3734 CB TYR B 894 11.738 −13.000 −37.387 1.00 53.49 ATOM 3735 CG TYR B 894 12.051 −14.469 −37.473 1.00 54.03 ATOM 3736 CD1 TYR B 894 12.231 −15.091 −38.706 1.00 54.75 ATOM 3737 CD2 TYR B 894 12.223 −15.228 −36.318 1.00 55.06 ATOM 3738 CE1 TYR B 894 12.580 −16.438 −38.784 1.00 57.69 ATOM 3739 CE2 TYR B 894 12.574 −16.571 −36.381 1.00 57.19 ATOM 3740 CZ TYR B 894 12.755 −17.175 −37.616 1.00 59.22 ATOM 3741 OH TYR B 894 13.136 −18.504 −37.679 1.00 61.11 ATOM 3742 N ARG B 895 11.623 −10.269 −38.405 1.00 53.26 ATOM 3743 CA ARG B 895 11.112 −8.912 −38.417 1.00 53.71 ATOM 3744 C ARG B 895 9.726 −8.838 −37.788 1.00 55.40 ATOM 3745 O ARG B 895 8.700 −8.972 −38.464 1.00 56.92 ATOM 3746 CB ARG B 895 11.066 −8.363 −39.840 1.00 52.60 ATOM 3747 CG ARG B 895 12.425 −8.042 −40.416 1.00 54.61 ATOM 3748 CD ARG B 895 12.326 −6.918 −41.439 1.00 56.13 ATOM 3749 NE ARG B 895 13.641 −6.505 −41.914 1.00 58.90 ATOM 3750 CZ ARG B 895 14.368 −7.200 −42.781 1.00 61.14 ATOM 3751 NH1 ARG B 895 13.894 −8.343 −43.271 1.00 61.94 ATOM 3752 NH2 ARG B 895 15.571 −6.767 −43.144 1.00 58.94 ATOM 3753 N ALA B 896 9.705 −8.634 −36.476 1.00 55.24 ATOM 3754 CA ALA B 896 8.452 −8.519 −35.748 1.00 53.33 ATOM 3755 C ALA B 896 8.350 −7.085 −35.215 1.00 51.36 ATOM 3756 O ALA B 896 8.063 −6.872 −34.040 1.00 51.66 ATOM 3757 CB ALA B 896 8.419 −9.536 −34.598 1.00 52.72 ATOM 3758 N PHE B 897 8.592 −6.104 −36.086 1.00 48.95 ATOM 3759 CA PHE B 897 8.535 −4.695 −35.683 1.00 46.93 ATOM 3760 C PHE B 897 7.134 −4.237 −35.300 1.00 44.17 ATOM 3761 O PHE B 897 6.209 −4.266 −36.106 1.00 42.11 ATOM 3762 CB PHE B 897 9.093 −3.785 −36.787 1.00 47.63 ATOM 3763 CG PHE B 897 10.572 −3.928 −36.993 1.00 50.51 ATOM 3764 CD1 PHE B 897 11.076 −4.474 −38.172 1.00 53.25 ATOM 3765 CD2 PHE B 897 11.465 −3.567 −35.988 1.00 50.87 ATOM 3766 CE1 PHE B 897 12.451 −4.662 −38.342 1.00 52.04 ATOM 3767 CE2 PHE B 897 12.835 −3.750 −36.148 1.00 50.84 ATOM 3768 CZ PHE B 897 13.329 −4.300 −37.326 1.00 52.35 ATOM 3769 N THR B 898 6.997 −3.798 −34.055 1.00 42.52 ATOM 3770 CA THR B 898 5.717 −3.352 −33.534 1.00 40.56 ATOM 3771 C THR B 898 5.916 −2.231 −32.543 1.00 39.82 ATOM 3772 O THR B 898 7.027 −1.983 −32.089 1.00 38.49 ATOM 3773 CB THR B 898 5.000 −4.480 −32.779 1.00 39.38 ATOM 3774 OG1 THR B 898 5.744 −4.803 −31.602 1.00 39.33 ATOM 3775 CG2 THR B 898 4.881 −5.711 −33.638 1.00 37.90 ATOM 3776 N HIS B 899 4.826 −1.558 −32.198 1.00 39.68 ATOM 3777 CA HIS B 899 4.907 −0.487 −31.225 1.00 40.57 ATOM 3778 C HIS B 899 5.672 −0.985 −29.998 1.00 39.75 ATOM 3779 O HIS B 899 6.494 −0.262 −29.433 1.00 40.90 ATOM 3780 CB HIS B 899 3.499 −0.040 −30.838 1.00 41.77 ATOM 3781 CG HIS B 899 2.711 0.476 −31.994 1.00 44.38 ATOM 3782 ND1 HIS B 899 3.136 1.539 −32.765 1.00 46.58 ATOM 3783 CD2 HIS B 899 1.560 0.042 −32.554 1.00 44.66 ATOM 3784 CE1 HIS B 899 2.283 1.734 −33.752 1.00 45.15 ATOM 3785 NE2 HIS B 899 1.317 0.838 −33.648 1.00 47.56 ATOM 3786 N GLN B 900 5.420 −2.227 −29.604 1.00 37.28 ATOM 3787 CA GLN B 900 6.100 −2.770 −28.452 1.00 38.27 ATOM 3788 C GLN B 900 7.608 −2.902 −28.658 1.00 38.64 ATOM 3789 O GLN B 900 8.374 −2.701 −27.717 1.00 39.27 ATOM 3790 CB GLN B 900 5.492 −4.112 −28.045 1.00 38.52 ATOM 3791 CG GLN B 900 4.165 −3.987 −27.302 1.00 39.82 ATOM 3792 CD GLN B 900 4.050 −2.696 −26.472 1.00 43.54 ATOM 3793 OE1 GLN B 900 3.859 −1.614 −27.025 1.00 46.46 ATOM 3794 NE2 GLN B 900 4.161 −2.812 −25.145 1.00 44.27 ATOM 3795 N SER B 901 8.048 −3.226 −29.872 1.00 36.36 ATOM 3796 CA SER B 901 9.482 −3.340 −30.110 1.00 35.93 ATOM 3797 C SER B 901 10.093 −1.938 −30.014 1.00 37.71 ATOM 3798 O SER B 901 11.239 −1.759 −29.584 1.00 35.11 ATOM 3799 CB SER B 901 9.773 −3.993 −31.472 1.00 35.40 ATOM 3800 OG SER B 901 9.213 −3.299 −32.566 1.00 35.60 ATOM 3801 N ASP B 902 9.302 −0.936 −30.387 1.00 36.58 ATOM 3802 CA ASP B 902 9.753 0.436 −30.297 1.00 35.05 ATOM 3803 C ASP B 902 9.918 0.797 −28.816 1.00 35.23 ATOM 3804 O ASP B 902 10.766 1.618 −28.453 1.00 31.03 ATOM 3805 CB ASP B 902 8.738 1.368 −30.961 1.00 35.87 ATOM 3806 CG ASP B 902 9.065 1.646 −32.421 1.00 38.00 ATOM 3807 OD1 ASP B 902 10.043 1.066 −32.944 1.00 35.01 ATOM 3808 OD2 ASP B 902 8.341 2.454 −33.043 1.00 40.53 ATOM 3809 N VAL B 903 9.112 0.179 −27.957 1.00 34.13 ATOM 3810 CA VAL B 903 9.214 0.479 −26.538 1.00 36.81 ATOM 3811 C VAL B 903 10.559 0.008 −26.010 1.00 37.63 ATOM 3812 O VAL B 903 11.184 0.674 −25.180 1.00 37.43 ATOM 3813 CB VAL B 903 8.075 −0.178 −25.727 1.00 38.45 ATOM 3814 CG1 VAL B 903 8.380 −0.100 −24.229 1.00 37.24 ATOM 3815 CG2 VAL B 903 6.763 0.533 −26.026 1.00 37.24 ATOM 3816 N TRP B 904 11.005 −1.144 −26.498 1.00 39.08 ATOM 3817 CA TRP B 904 12.297 −1.674 −26.092 1.00 37.59 ATOM 3818 C TRP B 904 13.332 −0.601 −26.441 1.00 34.67 ATOM 3819 O TRP B 904 14.129 −0.203 −25.602 1.00 32.68 ATOM 3820 CB TRP B 904 12.600 −2.980 −26.848 1.00 40.25 ATOM 3821 CG TRP B 904 13.943 −3.588 −26.523 1.00 41.50 ATOM 3822 CD1 TRP B 904 15.160 −3.031 −26.742 1.00 39.65 ATOM 3823 CD2 TRP B 904 14.190 −4.857 −25.891 1.00 43.17 ATOM 3824 NE1 TRP B 904 16.153 −3.861 −26.285 1.00 42.57 ATOM 3825 CE2 TRP B 904 15.588 −4.991 −25.759 1.00 43.45 ATOM 3826 CE3 TRP B 904 13.364 −5.892 −25.424 1.00 45.15 ATOM 3827 CZ2 TRP B 904 16.188 −6.123 −25.176 1.00 45.09 ATOM 3828 CZ3 TRP B 904 13.962 −7.024 −24.839 1.00 45.21 ATOM 3829 CH2 TRP B 904 15.360 −7.125 −24.724 1.00 44.37 ATOM 3830 N SER B 905 13.296 −0.123 −27.678 1.00 32.67 ATOM 3831 CA SER B 905 14.233 0.895 −28.120 1.00 34.81 ATOM 3832 C SER B 905 14.182 2.102 −27.190 1.00 35.70 ATOM 3833 O SER B 905 15.214 2.596 −26.727 1.00 35.81 ATOM 3834 CB SER B 905 13.904 1.309 −29.548 1.00 35.88 ATOM 3835 OG SER B 905 13.939 0.183 −30.404 1.00 34.89 ATOM 3836 N TYR B 906 12.963 2.556 −26.920 1.00 37.42 ATOM 3837 CA TYR B 906 12.712 3.679 −26.032 1.00 36.19 ATOM 3838 C TYR B 906 13.517 3.478 −24.763 1.00 36.71 ATOM 3839 O TYR B 906 14.208 4.378 −24.304 1.00 35.97 ATOM 3840 CB TYR B 906 11.226 3.741 −25.677 1.00 36.25 ATOM 3841 CG TYR B 906 10.889 4.865 −24.733 1.00 35.80 ATOM 3842 CD1 TYR B 906 10.571 6.130 −25.212 1.00 33.13 ATOM 3843 CD2 TYR B 906 10.983 4.683 −23.362 1.00 37.44 ATOM 3844 CE1 TYR B 906 10.369 7.183 −24.360 1.00 36.10 ATOM 3845 CE2 TYR B 906 10.782 5.738 −22.489 1.00 40.97 ATOM 3846 CZ TYR B 906 10.479 6.991 −22.994 1.00 39.58 ATOM 3847 OH TYR B 906 10.328 8.050 −22.125 1.00 39.67 ATOM 3848 N GLY B 907 13.409 2.289 −24.189 1.00 36.90 ATOM 3849 CA GLY B 907 14.150 1.995 −22.982 1.00 38.61 ATOM 3850 C GLY B 907 15.642 2.197 −23.171 1.00 41.80 ATOM 3851 O GLY B 907 16.285 2.870 −22.362 1.00 41.26 ATOM 3852 N VAL B 908 16.196 1.616 −24.238 1.00 43.21 ATOM 3853 CA VAL B 908 17.626 1.728 −24.527 1.00 42.16 ATOM 3854 C VAL B 908 17.967 3.191 −24.740 1.00 42.43 ATOM 3855 O VAL B 908 19.041 3.655 −24.358 1.00 42.57 ATOM 3856 CB VAL B 908 18.013 0.928 −25.794 1.00 43.20 ATOM 3857 CG1 VAL B 908 19.510 1.037 −26.052 1.00 42.14 ATOM 3858 CG2 VAL B 908 17.626 −0.525 −25.622 1.00 42.76 ATOM 3859 N THR B 909 17.034 3.919 −25.338 1.00 40.59 ATOM 3860 CA THR B 909 17.239 5.333 −25.583 1.00 40.05 ATOM 3861 C THR B 909 17.318 6.168 −24.318 1.00 41.07 ATOM 3862 O THR B 909 18.227 6.971 −24.180 1.00 44.18 ATOM 3863 CB THR B 909 16.133 5.925 −26.447 1.00 38.19 ATOM 3864 OG1 THR B 909 16.119 5.268 −27.717 1.00 37.26 ATOM 3865 CG2 THR B 909 16.375 7.413 −26.658 1.00 35.17 ATOM 3866 N ILE B 910 16.383 6.006 −23.390 1.00 41.77 ATOM 3867 CA ILE B 910 16.459 6.830 −22.191 1.00 44.01 ATOM 3868 C ILE B 910 17.678 6.440 −21.365 1.00 43.93 ATOM 3869 O ILE B 910 18.162 7.222 −20.537 1.00 43.25 ATOM 3870 CB ILE B 910 15.171 6.768 −21.323 1.00 44.35 ATOM 3871 CG1 ILE B 910 15.014 5.394 −20.688 1.00 45.86 ATOM 3872 CG2 ILE B 910 13.960 7.146 −22.179 1.00 44.14 ATOM 3873 CD1 ILE B 910 13.834 5.285 −19.766 1.00 45.31 ATOM 3874 N TRP B 911 18.179 5.233 −21.611 1.00 43.13 ATOM 3875 CA TRP B 911 19.369 4.746 −20.927 1.00 41.24 ATOM 3876 C TRP B 911 20.542 5.605 −21.424 1.00 41.42 ATOM 3877 O TRP B 911 21.375 6.032 −20.629 1.00 41.37 ATOM 3878 CB TRP B 911 19.600 3.279 −21.265 1.00 42.93 ATOM 3879 CG TRP B 911 20.768 2.671 −20.582 1.00 46.13 ATOM 3880 CD1 TRP B 911 20.778 2.044 −19.370 1.00 48.07 ATOM 3881 CD2 TRP B 911 22.120 2.647 −21.058 1.00 47.88 ATOM 3882 NE1 TRP B 911 22.053 1.629 −19.059 1.00 48.23 ATOM 3883 CE2 TRP B 911 22.897 1.988 −20.078 1.00 48.28 ATOM 3884 CE3 TRP B 911 22.751 3.123 −22.216 1.00 46.20 ATOM 3885 CZ2 TRP B 911 24.274 1.792 −20.221 1.00 45.73 ATOM 3886 CZ3 TRP B 911 24.120 2.928 −22.355 1.00 46.02 ATOM 3887 CH2 TRP B 911 24.865 2.268 −21.362 1.00 45.66 ATOM 3888 N GLU B 912 20.600 5.874 −22.728 1.00 40.12 ATOM 3889 CA GLU B 912 21.673 6.703 −23.263 1.00 42.28 ATOM 3890 C GLU B 912 21.616 8.051 −22.573 1.00 43.95 ATOM 3891 O GLU B 912 22.649 8.627 −22.228 1.00 45.55 ATOM 3892 CB GLU B 912 21.524 6.955 −24.759 1.00 41.44 ATOM 3893 CG GLU B 912 21.505 5.742 −25.635 1.00 44.81 ATOM 3894 CD GLU B 912 21.220 6.107 −27.081 1.00 47.97 ATOM 3895 OE1 GLU B 912 22.153 6.551 −27.790 1.00 44.98 ATOM 3896 OE2 GLU B 912 20.049 5.964 −27.502 1.00 50.02 ATOM 3897 N LEU B 913 20.402 8.558 −22.374 1.00 44.41 ATOM 3898 CA LEU B 913 20.235 9.857 −21.734 1.00 43.18 ATOM 3899 C LEU B 913 20.652 9.823 −20.270 1.00 43.99 ATOM 3900 O LEU B 913 21.414 10.675 −19.823 1.00 44.57 ATOM 3901 CB LEU B 913 18.787 10.332 −21.862 1.00 40.85 ATOM 3902 CG LEU B 913 18.216 10.396 −23.286 1.00 41.67 ATOM 3903 CD1 LEU B 913 16.795 10.945 −23.221 1.00 39.11 ATOM 3904 CD2 LEU B 913 19.089 11.283 −24.187 1.00 38.24 ATOM 3905 N MET B 914 20.158 8.843 −19.519 1.00 45.82 ATOM 3906 CA MET B 914 20.513 8.742 −18.109 1.00 48.13 ATOM 3907 C MET B 914 22.023 8.596 −17.917 1.00 48.88 ATOM 3908 O MET B 914 22.553 8.972 −16.864 1.00 48.55 ATOM 3909 CB MET B 914 19.796 7.564 −17.443 1.00 50.82 ATOM 3910 CG MET B 914 18.292 7.740 −17.317 1.00 52.72 ATOM 3911 SD MET B 914 17.787 9.437 −16.952 1.00 53.52 ATOM 3912 CE MET B 914 16.626 9.705 −18.264 1.00 52.21 ATOM 3913 N THR B 915 22.710 8.048 −18.923 1.00 47.30 ATOM 3914 CA THR B 915 24.163 7.892 −18.849 1.00 46.63 ATOM 3915 C THR B 915 24.875 9.052 −19.562 1.00 48.58 ATOM 3916 O THR B 915 26.059 8.968 −19.886 1.00 48.03 ATOM 3917 CB THR B 915 24.642 6.559 −19.474 1.00 44.86 ATOM 3918 OG1 THR B 915 24.277 6.516 −20.860 1.00 44.85 ATOM 3919 CG2 THR B 915 24.043 5.373 −18.737 1.00 42.30 ATOM 3920 N PHE B 916 24.148 10.135 −19.809 1.00 50.49 ATOM 3921 CA PHE B 916 24.731 11.297 −20.463 1.00 52.07 ATOM 3922 C PHE B 916 25.505 10.901 −21.717 1.00 54.08 ATOM 3923 O PHE B 916 26.687 11.222 −21.848 1.00 56.00 ATOM 3924 CB PHE B 916 25.669 12.010 −19.489 1.00 52.26 ATOM 3925 CG PHE B 916 24.972 12.617 −18.305 1.00 52.03 ATOM 3926 CD1 PHE B 916 24.174 13.747 −18.452 1.00 52.39 ATOM 3927 CD2 PHE B 916 25.128 12.076 −17.040 1.00 52.11 ATOM 3928 CE1 PHE B 916 23.547 14.329 −17.356 1.00 51.26 ATOM 3929 CE2 PHE B 916 24.502 12.654 −15.938 1.00 52.35 ATOM 3930 CZ PHE B 916 23.713 13.781 −16.097 1.00 50.17 ATOM 3931 N GLY B 917 24.845 10.188 −22.626 1.00 54.17 ATOM 3932 CA GLY B 917 25.489 9.772 −23.863 1.00 53.58 ATOM 3933 C GLY B 917 26.130 8.392 −23.882 1.00 54.28 ATOM 3934 O GLY B 917 26.799 8.047 −24.858 1.00 56.32 ATOM 3935 N GLY B 918 25.925 7.596 −22.834 1.00 52.63 ATOM 3936 CA GLY B 918 26.519 6.268 −22.777 1.00 51.85 ATOM 3937 C GLY B 918 26.302 5.358 −23.977 1.00 53.07 ATOM 3938 O GLY B 918 25.357 5.533 −24.748 1.00 53.60 ATOM 3939 N LYS B 919 27.184 4.375 −24.136 1.00 53.42 ATOM 3940 CA LYS B 919 27.083 3.430 −25.241 1.00 53.94 ATOM 3941 C LYS B 919 26.529 2.081 −24.777 1.00 54.09 ATOM 3942 O LYS B 919 27.059 1.461 −23.853 1.00 53.78 ATOM 3943 CB LYS B 919 28.451 3.224 −25.898 1.00 56.15 ATOM 3944 CG LYS B 919 29.088 4.504 −26.440 1.00 60.22 ATOM 3945 CD LYS B 919 30.229 4.199 −27.399 1.00 62.11 ATOM 3946 CE LYS B 919 29.703 3.490 −28.644 1.00 65.81 ATOM 3947 NZ LYS B 919 30.785 3.065 −29.581 1.00 68.08 ATOM 3948 N PRO B 920 25.449 1.609 −25.424 1.00 53.96 ATOM 3949 CA PRO B 920 24.779 0.340 −25.122 1.00 52.93 ATOM 3950 C PRO B 920 25.730 −0.832 −25.235 1.00 52.53 ATOM 3951 O PRO B 920 26.390 −0.994 −26.254 1.00 51.03 ATOM 3952 CB PRO B 920 23.685 0.259 −26.184 1.00 52.25 ATOM 3953 CG PRO B 920 23.412 1.669 −26.510 1.00 54.01 ATOM 3954 CD PRO B 920 24.783 2.283 −26.550 1.00 53.55 ATOM 3955 N TYR B 921 25.774 −1.658 −24.197 1.00 54.38 ATOM 3956 CA TYR B 921 26.649 −2.823 −24.182 1.00 57.62 ATOM 3957 C TYR B 921 28.007 −2.445 −24.764 1.00 60.38 ATOM 3958 O TYR B 921 28.491 −3.075 −25.707 1.00 61.02 ATOM 3959 CB TYR B 921 26.022 −3.958 −24.992 1.00 56.19 ATOM 3960 CG TYR B 921 24.546 −4.115 −24.735 1.00 53.82 ATOM 3961 CD1 TYR B 921 23.612 −3.483 −25.551 1.00 54.08 ATOM 3962 CD2 TYR B 921 24.084 −4.862 −23.658 1.00 51.52 ATOM 3963 CE1 TYR B 921 22.257 −3.588 −25.303 1.00 53.70 ATOM 3964 CE2 TYR B 921 22.730 −4.975 −23.396 1.00 52.18 ATOM 3965 CZ TYR B 921 21.820 −4.337 −24.223 1.00 53.77 ATOM 3966 OH TYR B 921 20.474 −4.454 −23.983 1.00 52.26 ATOM 3967 N ASP B 922 28.605 −1.409 −24.184 1.00 63.62 ATOM 3968 CA ASP B 922 29.895 −0.888 −24.616 1.00 67.06 ATOM 3969 C ASP B 922 30.960 −1.967 −24.783 1.00 68.44 ATOM 3970 O ASP B 922 31.239 −2.732 −23.857 1.00 67.06 ATOM 3971 CB ASP B 922 30.400 0.152 −23.616 1.00 69.17 ATOM 3972 CG ASP B 922 31.481 1.037 −24.200 1.00 70.95 ATOM 3973 OD1 ASP B 922 32.337 0.521 −24.957 1.00 72.34 ATOM 3974 OD2 ASP B 922 31.478 2.250 −23.894 1.00 70.84 ATOM 3975 N GLY B 923 31.556 −2.008 −25.971 1.00 70.59 ATOM 3976 CA GLY B 923 32.595 −2.980 −26.257 1.00 72.18 ATOM 3977 C GLY B 923 32.100 −4.329 −26.747 1.00 72.53 ATOM 3978 O GLY B 923 32.580 −4.834 −27.759 1.00 74.13 ATOM 3979 N ILE B 924 31.142 −4.909 −26.032 1.00 71.67 ATOM 3980 CA ILE B 924 30.591 −6.215 −26.373 1.00 70.50 ATOM 3981 C ILE B 924 30.351 −6.414 −27.872 1.00 71.43 ATOM 3982 O ILE B 924 29.838 −5.527 −28.556 1.00 71.73 ATOM 3983 CB ILE B 924 29.278 −6.462 −25.597 1.00 69.48 ATOM 3984 CG1 ILE B 924 29.545 −6.319 −24.091 1.00 68.05 ATOM 3985 CG2 ILE B 924 28.729 −7.850 −25.917 1.00 67.40 ATOM 3986 CD1 ILE B 924 28.299 −6.301 −23.212 1.00 69.45 ATOM 3987 N PRO B 925 30.737 −7.594 −28.398 1.00 71.75 ATOM 3988 CA PRO B 925 30.619 −8.024 −29.799 1.00 71.06 ATOM 3989 C PRO B 925 29.197 −8.007 −30.368 1.00 69.91 ATOM 3990 O PRO B 925 28.333 −8.764 −29.935 1.00 68.95 ATOM 3991 CB PRO B 925 31.191 −9.442 −29.774 1.00 71.99 ATOM 3992 CG PRO B 925 32.182 −9.390 −28.661 1.00 72.05 ATOM 3993 CD PRO B 925 31.432 −8.625 −27.604 1.00 72.02 ATOM 3994 N THR B 926 28.977 −7.158 −31.361 1.00 69.43 ATOM 3995 CA THR B 926 27.675 −7.030 −32.002 1.00 69.48 ATOM 3996 C THR B 926 26.961 −8.380 −32.208 1.00 69.75 ATOM 3997 O THR B 926 25.747 −8.486 −32.028 1.00 70.07 ATOM 3998 CB THR B 926 27.826 −6.287 −33.366 1.00 70.00 ATOM 3999 OG1 THR B 926 26.543 −6.131 −33.980 1.00 68.48 ATOM 4000 CG2 THR B 926 28.766 −7.055 −34.309 1.00 70.72 ATOM 4001 N ALA B 927 27.716 −9.412 −32.566 1.00 69.65 ATOM 4002 CA ALA B 927 27.140 −10.732 −32.804 1.00 68.51 ATOM 4003 C ALA B 927 26.683 −11.403 −31.510 1.00 68.30 ATOM 4004 O ALA B 927 25.807 −12.270 −31.526 1.00 68.58 ATOM 4005 CB ALA B 927 28.165 −11.626 −33.527 1.00 66.12 ATOM 4006 N GLU B 928 27.272 −10.992 −30.392 1.00 68.00 ATOM 4007 CA GLU B 928 26.958 −11.577 −29.090 1.00 68.38 ATOM 4008 C GLU B 928 25.634 −11.170 −28.463 1.00 66.53 ATOM 4009 O GLU B 928 25.007 −11.959 −27.753 1.00 64.89 ATOM 4010 CB GLU B 928 28.075 −11.270 −28.088 1.00 71.51 ATOM 4011 CG GLU B 928 29.263 −12.221 −28.136 1.00 75.50 ATOM 4012 CD GLU B 928 30.041 −12.231 −26.826 1.00 79.00 ATOM 4013 OE1 GLU B 928 30.933 −13.095 −26.662 1.00 81.12 ATOM 4014 OE2 GLU B 928 29.760 −11.374 −25.957 1.00 79.77 ATOM 4015 N ILE B 929 25.220 −9.936 −28.714 1.00 64.75 ATOM 4016 CA ILE B 929 23.987 −9.415 −28.147 1.00 63.35 ATOM 4017 C ILE B 929 22.858 −10.446 −28.077 1.00 63.03 ATOM 4018 O ILE B 929 22.337 −10.734 −26.998 1.00 61.05 ATOM 4019 CB ILE B 929 23.520 −8.184 −28.932 1.00 61.08 ATOM 4020 CG1 ILE B 929 24.652 −7.155 −28.994 1.00 58.47 ATOM 4021 CG2 ILE B 929 22.284 −7.600 −28.286 1.00 62.49 ATOM 4022 CD1 ILE B 929 25.199 −6.739 −27.651 1.00 53.78 ATOM 4023 N PRO B 930 22.474 −11.026 −29.225 1.00 63.06 ATOM 4024 CA PRO B 930 21.402 −12.024 −29.257 1.00 63.56 ATOM 4025 C PRO B 930 21.495 −13.082 −28.155 1.00 64.62 ATOM 4026 O PRO B 930 20.516 −13.350 −27.452 1.00 64.41 ATOM 4027 CB PRO B 930 21.541 −12.617 −30.652 1.00 62.01 ATOM 4028 CG PRO B 930 21.934 −11.428 −31.446 1.00 62.44 ATOM 4029 CD PRO B 930 22.998 −10.792 −30.581 1.00 61.86 ATOM 4030 N ASP B 931 22.668 −13.686 −28.004 1.00 65.47 ATOM 4031 CA ASP B 931 22.839 −14.703 −26.982 1.00 66.27 ATOM 4032 C ASP B 931 22.656 −14.072 −25.616 1.00 65.47 ATOM 4033 O ASP B 931 21.839 −14.537 −24.821 1.00 64.75 ATOM 4034 CB ASP B 931 24.227 −15.345 −27.078 1.00 70.06 ATOM 4035 CG ASP B 931 24.483 −16.356 −25.967 1.00 73.85 ATOM 4036 OD1 ASP B 931 23.678 −17.313 −25.835 1.00 75.74 ATOM 4037 OD2 ASP B 931 25.484 −16.189 −25.228 1.00 74.15 ATOM 4038 N LEU B 932 23.419 −13.011 −25.353 1.00 65.40 ATOM 4039 CA LEU B 932 23.349 −12.298 −24.080 1.00 65.25 ATOM 4040 C LEU B 932 21.902 −12.006 −23.678 1.00 65.94 ATOM 4041 O LEU B 932 21.452 −12.390 −22.594 1.00 65.04 ATOM 4042 CB LEU B 932 24.130 −10.982 −24.161 1.00 65.95 ATOM 4043 CG LEU B 932 25.660 −11.055 −24.245 1.00 68.42 ATOM 4044 CD1 LEU B 932 26.237 −9.642 −24.271 1.00 69.04 ATOM 4045 CD2 LEU B 932 26.219 −11.823 −23.044 1.00 68.73 ATOM 4046 N LEU B 933 21.173 −11.334 −24.562 1.00 65.07 ATOM 4047 CA LEU B 933 19.787 −10.989 −24.298 1.00 64.62 ATOM 4048 C LEU B 933 18.923 −12.152 −23.810 1.00 64.97 ATOM 4049 O LEU B 933 18.110 −11.980 −22.899 1.00 65.95 ATOM 4050 CB LEU B 933 19.166 −10.368 −25.548 1.00 63.72 ATOM 4051 CG LEU B 933 19.756 −9.012 −25.939 1.00 63.23 ATOM 4052 CD1 LEU B 933 19.177 −8.570 −27.271 1.00 61.73 ATOM 4053 CD2 LEU B 933 19.464 −7.986 −24.852 1.00 61.35 ATOM 4054 N GLU B 934 19.096 −13.331 −24.397 1.00 64.87 ATOM 4055 CA GLU B 934 18.294 −14.487 −23.997 1.00 65.11 ATOM 4056 C GLU B 934 18.805 −15.154 −22.730 1.00 63.75 ATOM 4057 O GLU B 934 18.163 −16.050 −22.199 1.00 63.55 ATOM 4058 CB GLU B 934 18.220 −15.494 −25.148 1.00 66.18 ATOM 4059 CG GLU B 934 17.478 −14.925 −26.342 1.00 71.36 ATOM 4060 CD GLU B 934 17.763 −15.642 −27.649 1.00 74.08 ATOM 4061 OE1 GLU B 934 18.950 −15.765 −28.029 1.00 75.67 ATOM 4062 OE2 GLU B 934 16.790 −16.066 −28.306 1.00 76.95 ATOM 4063 N LYS B 935 19.958 −14.705 −22.249 1.00 63.26 ATOM 4064 CA LYS B 935 20.558 −15.241 −21.032 1.00 63.78 ATOM 4065 C LYS B 935 20.263 −14.297 −19.867 1.00 64.04 ATOM 4066 O LYS B 935 20.830 −14.442 −18.783 1.00 65.10 ATOM 4067 CB LYS B 935 22.077 −15.366 −21.185 1.00 64.14 ATOM 4068 CG LYS B 935 22.556 −16.374 −22.206 1.00 65.76 ATOM 4069 CD LYS B 935 22.334 −17.790 −21.719 1.00 68.99 ATOM 4070 CE LYS B 935 23.035 −18.799 −22.610 1.00 70.04 ATOM 4071 NZ LYS B 935 22.771 −20.184 −22.139 1.00 71.50 ATOM 4072 N GLY B 936 19.406 −13.308 −20.105 1.00 62.82 ATOM 4073 CA GLY B 936 19.055 −12.373 −19.051 1.00 61.39 ATOM 4074 C GLY B 936 19.872 −11.097 −18.997 1.00 60.41 ATOM 4075 O GLY B 936 19.600 −10.219 −18.185 1.00 60.95 ATOM 4076 N GLU B 937 20.875 −10.987 −19.857 1.00 59.63 ATOM 4077 CA GLU B 937 21.729 −9.797 −19.903 1.00 58.26 ATOM 4078 C GLU B 937 20.903 −8.522 −20.150 1.00 56.06 ATOM 4079 O GLU B 937 20.057 −8.496 −21.038 1.00 55.96 ATOM 4080 CB GLU B 937 22.757 −9.958 −21.033 1.00 58.85 ATOM 4081 CG GLU B 937 23.808 −8.877 −21.113 1.00 61.46 ATOM 4082 CD GLU B 937 24.884 −9.045 −20.069 1.00 64.22 ATOM 4083 OE1 GLU B 937 25.719 −8.129 −19.921 1.00 66.78 ATOM 4084 OE2 GLU B 937 24.900 −10.099 −19.401 1.00 66.18 ATOM 4085 N ARG B 938 21.135 −7.474 −19.366 1.00 53.07 ATOM 4086 CA ARG B 938 20.427 −6.213 −19.567 1.00 51.85 ATOM 4087 C ARG B 938 21.322 −5.046 −19.211 1.00 52.49 ATOM 4088 O ARG B 938 22.249 −5.179 −18.405 1.00 54.14 ATOM 4089 CB ARG B 938 19.154 −6.132 −18.728 1.00 49.08 ATOM 4090 CG ARG B 938 18.047 −7.023 −19.212 1.00 48.98 ATOM 4091 CD ARG B 938 17.653 −6.678 −20.629 1.00 51.23 ATOM 4092 NE ARG B 938 17.145 −7.859 −21.322 1.00 56.53 ATOM 4093 CZ ARG B 938 16.012 −8.471 −21.015 1.00 57.01 ATOM 4094 NH1 ARG B 938 15.267 −8.003 −20.025 1.00 62.70 ATOM 4095 NH2 ARG B 938 15.631 −9.549 −21.682 1.00 55.07 ATOM 4096 N LEU B 939 21.043 −3.898 −19.813 1.00 50.95 ATOM 4097 CA LEU B 939 21.832 −2.715 −19.547 1.00 51.34 ATOM 4098 C LEU B 939 21.867 −2.401 −18.049 1.00 51.66 ATOM 4099 O LEU B 939 20.869 −2.544 −17.343 1.00 50.27 ATOM 4100 CB LEU B 939 21.282 −1.534 −20.349 1.00 49.96 ATOM 4101 CG LEU B 939 21.558 −1.689 −21.849 1.00 49.98 ATOM 4102 CD1 LEU B 939 20.779 −0.666 −22.664 1.00 47.22 ATOM 4103 CD2 LEU B 939 23.050 −1.561 −22.078 1.00 47.98 ATOM 4104 N PRO B 940 23.038 −1.976 −17.549 1.00 51.95 ATOM 4105 CA PRO B 940 23.306 −1.620 −16.151 1.00 51.29 ATOM 4106 C PRO B 940 22.397 −0.511 −15.667 1.00 51.06 ATOM 4107 O PRO B 940 21.776 0.173 −16.469 1.00 52.57 ATOM 4108 CB PRO B 940 24.751 −1.146 −16.184 1.00 50.42 ATOM 4109 CG PRO B 940 25.325 −1.852 −17.362 1.00 52.89 ATOM 4110 CD PRO B 940 24.233 −1.750 −18.376 1.00 50.94 ATOM 4111 N GLN B 941 22.343 −0.324 −14.354 1.00 50.66 ATOM 4112 CA GLN B 941 21.535 0.725 −13.760 1.00 48.49 ATOM 4113 C GLN B 941 22.339 2.010 −13.777 1.00 46.91 ATOM 4114 O GLN B 941 23.409 2.089 −13.200 1.00 47.29 ATOM 4115 CB GLN B 941 21.151 0.357 −12.324 1.00 48.25 ATOM 4116 CG GLN B 941 20.480 1.481 −11.554 1.00 49.45 ATOM 4117 CD GLN B 941 19.811 1.011 −10.271 1.00 52.87 ATOM 4118 OE1 GLN B 941 19.261 1.815 −9.512 1.00 52.38 ATOM 4119 NE2 GLN B 941 19.842 −0.296 −10.026 1.00 55.49 ATOM 4120 N PRO B 942 21.838 3.038 −14.460 1.00 48.21 ATOM 4121 CA PRO B 942 22.613 4.278 −14.477 1.00 49.11 ATOM 4122 C PRO B 942 22.849 4.807 −13.059 1.00 50.71 ATOM 4123 O PRO B 942 21.954 4.803 −12.216 1.00 51.40 ATOM 4124 CB PRO B 942 21.745 5.216 −15.315 1.00 46.82 ATOM 4125 CG PRO B 942 21.020 4.271 −16.223 1.00 47.86 ATOM 4126 CD PRO B 942 20.629 3.159 −15.289 1.00 45.98 ATOM 4127 N PRO B 943 24.070 5.264 −12.782 1.00 51.83 ATOM 4128 CA PRO B 943 24.474 5.807 −11.484 1.00 51.12 ATOM 4129 C PRO B 943 23.470 6.802 −10.898 1.00 51.11 ATOM 4130 O PRO B 943 23.110 6.713 −9.723 1.00 51.29 ATOM 4131 CB PRO B 943 25.803 6.482 −11.805 1.00 52.65 ATOM 4132 CG PRO B 943 26.371 5.605 −12.856 1.00 52.13 ATOM 4133 CD PRO B 943 25.183 5.320 −13.744 1.00 52.53 ATOM 4134 N ILE B 944 23.028 7.748 −11.726 1.00 50.00 ATOM 4135 CA ILE B 944 22.099 8.792 −11.299 1.00 48.49 ATOM 4136 C ILE B 944 20.658 8.315 −11.174 1.00 49.21 ATOM 4137 O ILE B 944 19.785 9.043 −10.681 1.00 49.19 ATOM 4138 CB ILE B 944 22.117 9.983 −12.291 1.00 48.25 ATOM 4139 CG1 ILE B 944 21.350 9.618 −13.571 1.00 43.64 ATOM 4140 CG2 ILE B 944 23.557 10.345 −12.625 1.00 45.88 ATOM 4141 CD1 ILE B 944 21.185 10.768 −14.509 1.00 44.55 ATOM 4142 N CYS B 945 20.414 7.091 −11.623 1.00 49.20 ATOM 4143 CA CYS B 945 19.076 6.532 −11.595 1.00 50.25 ATOM 4144 C CYS B 945 18.623 6.005 −10.260 1.00 50.70 ATOM 4145 O CYS B 945 19.357 5.323 −9.553 1.00 53.59 ATOM 4146 CB CYS B 945 18.933 5.413 −12.630 1.00 50.33 ATOM 4147 SG CYS B 945 18.662 5.990 −14.307 1.00 50.97 ATOM 4148 N THR B 946 17.388 6.339 −9.930 1.00 49.35 ATOM 4149 CA THR B 946 16.765 5.883 −8.710 1.00 49.02 ATOM 4150 C THR B 946 16.161 4.554 −9.197 1.00 48.52 ATOM 4151 O THR B 946 15.777 4.457 −10.360 1.00 49.59 ATOM 4152 CB THR B 946 15.682 6.905 −8.282 1.00 46.42 ATOM 4153 OG1 THR B 946 15.473 6.829 −6.872 1.00 47.27 ATOM 4154 CG2 THR B 946 14.386 6.650 −9.002 1.00 43.71 ATOM 4155 N ILE B 947 16.100 3.527 −8.357 1.00 48.32 ATOM 4156 CA ILE B 947 15.546 2.252 −8.821 1.00 48.32 ATOM 4157 C ILE B 947 14.151 2.434 −9.422 1.00 48.84 ATOM 4158 O ILE B 947 13.685 1.600 −10.196 1.00 49.30 ATOM 4159 CB ILE B 947 15.478 1.180 −7.696 1.00 46.78 ATOM 4160 CG1 ILE B 947 15.096 −0.176 −8.312 1.00 49.09 ATOM 4161 CG2 ILE B 947 14.467 1.593 −6.627 1.00 46.28 ATOM 4162 CD1 ILE B 947 15.017 −1.363 −7.331 1.00 49.14 ATOM 4163 N ASP B 948 13.491 3.532 −9.075 1.00 49.00 ATOM 4164 CA ASP B 948 12.162 3.808 −9.611 1.00 50.27 ATOM 4165 C ASP B 948 12.247 3.963 −11.134 1.00 49.29 ATOM 4166 O ASP B 948 11.403 3.440 −11.874 1.00 48.74 ATOM 4167 CB ASP B 948 11.602 5.098 −9.002 1.00 53.06 ATOM 4168 CG ASP B 948 11.377 4.995 −7.503 1.00 53.88 ATOM 4169 OD1 ASP B 948 10.208 4.869 −7.094 1.00 54.68 ATOM 4170 OD2 ASP B 948 12.363 5.044 −6.736 1.00 55.07 ATOM 4171 N VAL B 949 13.272 4.691 −11.583 1.00 47.43 ATOM 4172 CA VAL B 949 13.515 4.940 −13.001 1.00 45.11 ATOM 4173 C VAL B 949 14.030 3.686 −13.692 1.00 46.35 ATOM 4174 O VAL B 949 13.546 3.304 −14.767 1.00 46.15 ATOM 4175 CB VAL B 949 14.576 6.043 −13.208 1.00 44.06 ATOM 4176 CG1 VAL B 949 14.835 6.254 −14.696 1.00 41.72 ATOM 4177 CG2 VAL B 949 14.128 7.325 −12.565 1.00 40.72 ATOM 4178 N TYR B 950 15.019 3.050 −13.068 1.00 46.25 ATOM 4179 CA TYR B 950 15.613 1.850 −13.629 1.00 46.35 ATOM 4180 C TYR B 950 14.590 0.760 −13.932 1.00 45.76 ATOM 4181 O TYR B 950 14.665 0.122 −14.977 1.00 43.83 ATOM 4182 CB TYR B 950 16.689 1.297 −12.694 1.00 46.54 ATOM 4183 CG TYR B 950 17.528 0.203 −13.325 1.00 49.48 ATOM 4184 CD1 TYR B 950 18.209 0.422 −14.524 1.00 48.95 ATOM 4185 CD2 TYR B 950 17.649 −1.050 −12.721 1.00 51.79 ATOM 4186 CE1 TYR B 950 18.986 −0.571 −15.105 1.00 49.83 ATOM 4187 CE2 TYR B 950 18.428 −2.057 −13.294 1.00 51.29 ATOM 4188 CZ TYR B 950 19.096 −1.809 −14.485 1.00 51.48 ATOM 4189 OH TYR B 950 19.891 −2.785 −15.041 1.00 49.38 ATOM 4190 N MET B 951 13.636 0.547 −13.030 1.00 46.47 ATOM 4191 CA MET B 951 12.630 −0.484 −13.258 1.00 47.95 ATOM 4192 C MET B 951 11.790 −0.156 −14.480 1.00 47.93 ATOM 4193 O MET B 951 11.274 −1.059 −15.152 1.00 50.04 ATOM 4194 CB MET B 951 11.741 −0.679 −12.026 1.00 49.33 ATOM 4195 CG MET B 951 12.514 −1.169 −10.798 1.00 55.37 ATOM 4196 SD MET B 951 13.753 −2.470 −11.188 1.00 62.22 ATOM 4197 CE MET B 951 12.677 −3.817 −11.608 1.00 59.62 ATOM 4198 N VAL B 952 11.650 1.128 −14.784 1.00 45.24 ATOM 4199 CA VAL B 952 10.896 1.494 −15.971 1.00 44.94 ATOM 4200 C VAL B 952 11.668 0.969 −17.194 1.00 44.46 ATOM 4201 O VAL B 952 11.113 0.260 −18.037 1.00 42.31 ATOM 4202 CB VAL B 952 10.694 3.031 −16.067 1.00 44.63 ATOM 4203 CG1 VAL B 952 10.122 3.407 −17.423 1.00 40.56 ATOM 4204 CG2 VAL B 952 9.738 3.489 −14.971 1.00 42.36 ATOM 4205 N MET B 953 12.954 1.300 −17.269 1.00 44.54 ATOM 4206 CA MET B 953 13.789 0.846 −18.377 1.00 45.71 ATOM 4207 C MET B 953 13.760 −0.677 −18.498 1.00 45.34 ATOM 4208 O MET B 953 13.606 −1.218 −19.598 1.00 44.65 ATOM 4209 CB MET B 953 15.227 1.307 −18.179 1.00 46.83 ATOM 4210 CG MET B 953 15.396 2.800 −18.224 1.00 52.42 ATOM 4211 SD MET B 953 16.973 3.296 −17.565 1.00 57.82 ATOM 4212 CE MET B 953 16.787 5.046 −17.587 1.00 57.27 ATOM 4213 N VAL B 954 13.903 −1.365 −17.369 1.00 43.09 ATOM 4214 CA VAL B 954 13.891 −2.815 −17.375 1.00 43.36 ATOM 4215 C VAL B 954 12.588 −3.343 −17.961 1.00 43.58 ATOM 4216 O VAL B 954 12.605 −4.189 −18.857 1.00 41.66 ATOM 4217 CB VAL B 954 14.094 −3.379 −15.961 1.00 43.56 ATOM 4218 CG1 VAL B 954 14.037 −4.883 −15.993 1.00 45.22 ATOM 4219 CG2 VAL B 954 15.439 −2.946 −15.430 1.00 44.09 ATOM 4220 N LYS B 955 11.459 −2.827 −17.476 1.00 44.30 ATOM 4221 CA LYS B 955 10.158 −3.262 −17.982 1.00 44.82 ATOM 4222 C LYS B 955 10.096 −3.192 −19.504 1.00 44.68 ATOM 4223 O LYS B 955 9.542 −4.072 −20.160 1.00 46.69 ATOM 4224 CB LYS B 955 9.041 −2.410 −17.391 1.00 46.61 ATOM 4225 CG LYS B 955 8.647 −2.770 −15.972 1.00 46.76 ATOM 4226 CD LYS B 955 7.588 −1.812 −15.500 1.00 47.23 ATOM 4227 CE LYS B 955 7.121 −2.128 −14.119 1.00 48.72 ATOM 4228 NZ LYS B 955 6.636 −0.872 −13.502 1.00 52.38 ATOM 4229 N CYS B 956 10.665 −2.139 −20.066 1.00 43.75 ATOM 4230 CA CYS B 956 10.682 −1.978 −21.509 1.00 43.94 ATOM 4231 C CYS B 956 11.396 −3.138 −22.195 1.00 45.19 ATOM 4232 O CYS B 956 11.205 −3.365 −23.397 1.00 43.93 ATOM 4233 CB CYS B 956 11.410 −0.692 −21.883 1.00 42.14 ATOM 4234 SG CYS B 956 10.593 0.788 −21.373 1.00 41.02 ATOM 4235 N TRP B 957 12.221 −3.860 −21.433 1.00 44.92 ATOM 4236 CA TRP B 957 12.995 −4.957 −21.995 1.00 45.41 ATOM 4237 C TRP B 957 12.543 −6.352 −21.592 1.00 47.76 ATOM 4238 O TRP B 957 13.328 −7.295 −21.641 1.00 47.21 ATOM 4239 CB TRP B 957 14.477 −4.783 −21.645 1.00 41.77 ATOM 4240 CG TRP B 957 15.012 −3.417 −21.957 1.00 38.80 ATOM 4241 CD1 TRP B 957 14.764 −2.680 −23.074 1.00 38.90 ATOM 4242 CD2 TRP B 957 15.910 −2.633 −21.150 1.00 37.82 ATOM 4243 NE1 TRP B 957 15.444 −1.482 −23.019 1.00 39.19 ATOM 4244 CE2 TRP B 957 16.159 −1.429 −21.851 1.00 37.54 ATOM 4245 CE3 TRP B 957 16.528 −2.832 −19.907 1.00 36.20 ATOM 4246 CZ2 TRP B 957 17.004 −0.425 −21.353 1.00 36.54 ATOM 4247 CZ3 TRP B 957 17.366 −1.835 −19.414 1.00 39.57 ATOM 4248 CH2 TRP B 957 17.596 −0.643 −20.142 1.00 36.55 ATOM 4249 N MET B 958 11.289 −6.491 −21.185 1.00 49.98 ATOM 4250 CA MET B 958 10.793 −7.810 −20.828 1.00 50.86 ATOM 4251 C MET B 958 10.806 −8.612 −22.115 1.00 50.79 ATOM 4252 O MET B 958 10.734 −8.045 −23.205 1.00 49.90 ATOM 4253 CB MET B 958 9.373 −7.731 −20.264 1.00 52.90 ATOM 4254 CG MET B 958 9.295 −7.075 −18.896 1.00 55.44 ATOM 4255 SD MET B 958 10.524 −7.763 −17.765 1.00 57.70 ATOM 4256 CE MET B 958 9.531 −9.050 −16.941 1.00 59.85 ATOM 4257 N ILE B 959 10.914 −9.927 −21.998 1.00 51.99 ATOM 4258 CA ILE B 959 10.955 −10.768 −23.184 1.00 53.60 ATOM 4259 C ILE B 959 9.611 −10.696 −23.888 1.00 52.84 ATOM 4260 O ILE B 959 9.536 −10.632 −25.111 1.00 52.06 ATOM 4261 CB ILE B 959 11.251 −12.232 −22.823 1.00 55.50 ATOM 4262 CG1 ILE B 959 12.621 −12.335 −22.135 1.00 59.93 ATOM 4263 CG2 ILE B 959 11.235 −13.079 −24.090 1.00 56.33 ATOM 4264 CD1 ILE B 959 12.904 −13.710 −21.482 1.00 62.42 ATOM 4265 N ASP B 960 8.551 −10.695 −23.093 1.00 53.61 ATOM 4266 CA ASP B 960 7.192 −10.625 −23.610 1.00 54.49 ATOM 4267 C ASP B 960 6.860 −9.199 −24.063 1.00 52.87 ATOM 4268 O ASP B 960 6.711 −8.290 −23.250 1.00 50.14 ATOM 4269 CB ASP B 960 6.212 −11.072 −22.528 1.00 57.08 ATOM 4270 CG ASP B 960 4.851 −11.400 −23.081 1.00 61.48 ATOM 4271 OD1 ASP B 960 4.233 −10.509 −23.706 1.00 65.36 ATOM 4272 OD2 ASP B 960 4.395 −12.550 −22.891 1.00 64.23 ATOM 4273 N ALA B 961 6.745 −9.020 −25.371 1.00 52.25 ATOM 4274 CA ALA B 961 6.438 −7.722 −25.950 1.00 53.15 ATOM 4275 C ALA B 961 5.192 −7.090 −25.339 1.00 54.47 ATOM 4276 O ALA B 961 5.188 −5.902 −25.013 1.00 54.47 ATOM 4277 CB ALA B 961 6.263 −7.864 −27.449 1.00 49.84 ATOM 4278 N ASP B 962 4.140 −7.888 −25.182 1.00 56.23 ATOM 4279 CA ASP B 962 2.888 −7.393 −24.618 1.00 57.94 ATOM 4280 C ASP B 962 2.943 −7.036 −23.135 1.00 56.89 ATOM 4281 O ASP B 962 2.045 −6.358 −22.632 1.00 57.51 ATOM 4282 CB ASP B 962 1.748 −8.396 −24.840 1.00 60.84 ATOM 4283 CG ASP B 962 1.280 −8.451 −26.289 1.00 64.87 ATOM 4284 OD1 ASP B 962 1.123 −7.376 −26.915 1.00 66.69 ATOM 4285 OD2 ASP B 962 1.054 −9.575 −26.794 1.00 67.24 ATOM 4286 N SER B 963 3.973 −7.481 −22.422 1.00 54.15 ATOM 4287 CA SER B 963 4.050 −7.144 −21.008 1.00 52.47 ATOM 4288 C SER B 963 4.973 −5.954 −20.761 1.00 50.73 ATOM 4289 O SER B 963 5.319 −5.646 −19.623 1.00 51.91 ATOM 4290 CB SER B 963 4.502 −8.354 −20.188 1.00 53.91 ATOM 4291 OG SER B 963 5.814 −8.753 −20.531 1.00 56.30 ATOM 4292 N ARG B 964 5.380 −5.288 −21.835 1.00 48.87 ATOM 4293 CA ARG B 964 6.235 −4.115 −21.710 1.00 47.43 ATOM 4294 C ARG B 964 5.327 −2.916 −21.536 1.00 45.64 ATOM 4295 O ARG B 964 4.202 −2.898 −22.036 1.00 46.22 ATOM 4296 CB ARG B 964 7.079 −3.914 −22.964 1.00 46.37 ATOM 4297 CG ARG B 964 8.058 −5.025 −23.230 1.00 47.48 ATOM 4298 CD ARG B 964 8.697 −4.888 −24.604 1.00 46.80 ATOM 4299 NE ARG B 964 9.474 −6.074 −24.930 1.00 47.04 ATOM 4300 CZ ARG B 964 9.889 −6.388 −26.149 1.00 46.77 ATOM 4301 NH1 ARG B 964 9.609 −5.600 −27.174 1.00 46.76 ATOM 4302 NH2 ARG B 964 10.564 −7.507 −26.343 1.00 48.41 ATOM 4303 N PRO B 965 5.800 −1.890 −20.831 1.00 43.80 ATOM 4304 CA PRO B 965 4.915 −0.733 −20.671 1.00 43.62 ATOM 4305 C PRO B 965 4.533 −0.150 −22.022 1.00 42.50 ATOM 4306 O PRO B 965 5.260 −0.301 −23.005 1.00 43.40 ATOM 4307 CB PRO B 965 5.743 0.226 −19.821 1.00 42.89 ATOM 4308 CG PRO B 965 7.161 −0.156 −20.152 1.00 45.29 ATOM 4309 CD PRO B 965 7.122 −1.653 −20.233 1.00 43.22 ATOM 4310 N LYS B 966 3.373 0.490 −22.080 1.00 40.83 ATOM 4311 CA LYS B 966 2.932 1.102 −23.313 1.00 40.21 ATOM 4312 C LYS B 966 3.289 2.583 −23.303 1.00 39.83 ATOM 4313 O LYS B 966 3.423 3.189 −22.232 1.00 38.40 ATOM 4314 CB LYS B 966 1.446 0.861 −23.491 1.00 41.77 ATOM 4315 CG LYS B 966 1.194 −0.588 −23.796 1.00 47.30 ATOM 4316 CD LYS B 966 −0.223 −0.888 −24.170 1.00 51.96 ATOM 4317 CE LYS B 966 −0.392 −2.395 −24.327 1.00 57.53 ATOM 4318 NZ LYS B 966 −1.831 −2.804 −24.235 1.00 61.18 ATOM 4319 N PHE B 967 3.469 3.167 −24.485 1.00 38.02 ATOM 4320 CA PHE B 967 3.866 4.569 −24.547 1.00 40.61 ATOM 4321 C PHE B 967 2.998 5.514 −23.741 1.00 41.52 ATOM 4322 O PHE B 967 3.509 6.479 −23.180 1.00 42.24 ATOM 4323 CB PHE B 967 4.007 5.032 −26.004 1.00 38.99 ATOM 4324 CG PHE B 967 5.289 4.572 −26.648 1.00 38.22 ATOM 4325 CD1 PHE B 967 5.279 3.891 −27.858 1.00 37.36 ATOM 4326 CD2 PHE B 967 6.510 4.769 −26.002 1.00 37.25 ATOM 4327 CE1 PHE B 967 6.477 3.405 −28.417 1.00 42.23 ATOM 4328 CE2 PHE B 967 7.712 4.287 −26.551 1.00 39.11 ATOM 4329 CZ PHE B 967 7.698 3.605 −27.756 1.00 39.07 ATOM 4330 N ALA B 968 1.701 5.223 −23.652 1.00 42.04 ATOM 4331 CA ALA B 968 0.792 6.059 −22.872 1.00 44.04 ATOM 4332 C ALA B 968 1.210 6.066 −21.398 1.00 46.45 ATOM 4333 O ALA B 968 1.146 7.098 −20.729 1.00 46.84 ATOM 4334 CB ALA B 968 −0.650 5.549 −22.998 1.00 42.69 ATOM 4335 N GLU B 969 1.640 4.913 −20.895 1.00 46.92 ATOM 4336 CA GLU B 969 2.048 4.804 −19.503 1.00 47.61 ATOM 4337 C GLU B 969 3.420 5.396 −19.227 1.00 47.48 ATOM 4338 O GLU B 969 3.637 6.015 −18.182 1.00 47.99 ATOM 4339 CB GLU B 969 2.079 3.349 −19.065 1.00 51.22 ATOM 4340 CG GLU B 969 0.851 2.539 −19.384 1.00 57.69 ATOM 4341 CD GLU B 969 1.087 1.070 −19.086 1.00 62.44 ATOM 4342 OE1 GLU B 969 1.928 0.442 −19.771 1.00 63.17 ATOM 4343 OE2 GLU B 969 0.446 0.546 −18.151 1.00 68.35 ATOM 4344 N LEU B 970 4.362 5.182 −20.138 1.00 45.82 ATOM 4345 CA LEU B 970 5.699 5.704 −19.917 1.00 44.09 ATOM 4346 C LEU B 970 5.597 7.211 −19.807 1.00 44.59 ATOM 4347 O LEU B 970 6.152 7.819 −18.890 1.00 45.03 ATOM 4348 CB LEU B 970 6.645 5.276 −21.050 1.00 43.43 ATOM 4349 CG LEU B 970 7.053 3.782 −21.016 1.00 43.26 ATOM 4350 CD1 LEU B 970 7.660 3.340 −22.331 1.00 40.75 ATOM 4351 CD2 LEU B 970 8.029 3.551 −19.887 1.00 40.19 ATOM 4352 N ALA B 971 4.849 7.815 −20.718 1.00 44.94 ATOM 4353 CA ALA B 971 4.684 9.257 −20.690 1.00 45.01 ATOM 4354 C ALA B 971 4.093 9.663 −19.350 1.00 46.07 ATOM 4355 O ALA B 971 4.559 10.602 −18.709 1.00 48.26 ATOM 4356 CB ALA B 971 3.782 9.699 −21.806 1.00 43.14 ATOM 4357 N ALA B 972 3.075 8.939 −18.919 1.00 43.91 ATOM 4358 CA ALA B 972 2.435 9.242 −17.660 1.00 46.47 ATOM 4359 C ALA B 972 3.386 9.110 −16.466 1.00 48.41 ATOM 4360 O ALA B 972 3.481 10.018 −15.635 1.00 50.02 ATOM 4361 CB ALA B 972 1.233 8.339 −17.474 1.00 46.27 ATOM 4362 N GLU B 973 4.092 7.988 −16.377 1.00 49.34 ATOM 4363 CA GLU B 973 5.003 7.768 −15.259 1.00 50.14 ATOM 4364 C GLU B 973 6.160 8.769 −15.233 1.00 49.00 ATOM 4365 O GLU B 973 6.488 9.309 −14.182 1.00 47.51 ATOM 4366 CB GLU B 973 5.537 6.330 −15.295 1.00 53.73 ATOM 4367 CG GLU B 973 6.424 5.917 −14.120 1.00 58.85 ATOM 4368 CD GLU B 973 5.733 6.039 −12.764 1.00 64.87 ATOM 4369 OE1 GLU B 973 4.555 5.625 −12.644 1.00 67.25 ATOM 4370 OE2 GLU B 973 6.374 6.540 −11.808 1.00 67.54 ATOM 4371 N PHE B 974 6.784 9.026 −16.376 1.00 47.15 ATOM 4372 CA PHE B 974 7.892 9.970 −16.385 1.00 46.71 ATOM 4373 C PHE B 974 7.340 11.351 −16.178 1.00 47.30 ATOM 4374 O PHE B 974 8.017 12.242 −15.672 1.00 45.15 ATOM 4375 CB PHE B 974 8.649 9.898 −17.700 1.00 44.76 ATOM 4376 CG PHE B 974 9.648 8.794 −17.742 1.00 45.39 ATOM 4377 CD1 PHE B 974 10.790 8.851 −16.952 1.00 43.84 ATOM 4378 CD2 PHE B 974 9.433 7.669 −18.533 1.00 44.99 ATOM 4379 CE1 PHE B 974 11.705 7.800 −16.946 1.00 43.56 ATOM 4380 CE2 PHE B 974 10.343 6.612 −18.531 1.00 44.73 ATOM 4381 CZ PHE B 974 11.480 6.680 −17.734 1.00 43.10 ATOM 4382 N SER B 975 6.082 11.509 −16.564 1.00 48.14 ATOM 4383 CA SER B 975 5.393 12.775 −16.427 1.00 48.35 ATOM 4384 C SER B 975 5.302 13.184 −14.953 1.00 48.95 ATOM 4385 O SER B 975 5.666 14.305 −14.589 1.00 49.88 ATOM 4386 CB SER B 975 3.999 12.661 −17.040 1.00 48.77 ATOM 4387 OG SER B 975 3.325 13.899 −17.030 1.00 52.34 ATOM 4388 N ARG B 976 4.831 12.287 −14.093 1.00 47.45 ATOM 4389 CA ARG B 976 4.732 12.658 −12.697 1.00 47.19 ATOM 4390 C ARG B 976 6.105 12.708 −12.029 1.00 47.91 ATOM 4391 O ARG B 976 6.298 13.433 −11.055 1.00 48.07 ATOM 4392 CB ARG B 976 3.771 11.721 −11.942 1.00 47.00 ATOM 4393 CG ARG B 976 4.268 10.343 −11.695 1.00 48.59 ATOM 4394 CD ARG B 976 3.392 9.578 −10.696 1.00 51.30 ATOM 4395 NE ARG B 976 4.049 8.319 −10.349 1.00 53.72 ATOM 4396 CZ ARG B 976 5.139 8.240 −9.593 1.00 56.06 ATOM 4397 NH1 ARG B 976 5.697 7.066 −9.337 1.00 58.55 ATOM 4398 NH2 ARG B 976 5.652 9.337 −9.056 1.00 57.80 ATOM 4399 N MET B 977 7.065 11.960 −12.558 1.00 49.05 ATOM 4400 CA MET B 977 8.407 11.967 −11.988 1.00 51.32 ATOM 4401 C MET B 977 9.021 13.332 −12.249 1.00 52.43 ATOM 4402 O MET B 977 9.887 13.796 −11.503 1.00 52.50 ATOM 4403 CB MET B 977 9.269 10.854 −12.604 1.00 52.10 ATOM 4404 CG MET B 977 9.056 9.489 −11.939 1.00 54.48 ATOM 4405 SD MET B 977 9.708 8.090 −12.871 1.00 54.18 ATOM 4406 CE MET B 977 11.338 8.258 −12.532 1.00 54.40 ATOM 4407 N ALA B 978 8.548 13.981 −13.309 1.00 53.20 ATOM 4408 CA ALA B 978 9.030 15.303 −13.672 1.00 52.59 ATOM 4409 C ALA B 978 8.429 16.332 −12.714 1.00 53.53 ATOM 4410 O ALA B 978 8.910 17.468 −12.625 1.00 53.68 ATOM 4411 CB ALA B 978 8.647 15.621 −15.112 1.00 49.91 ATOM 4412 N ARG B 979 7.379 15.936 −11.999 1.00 53.98 ATOM 4413 CA ARG B 979 6.749 16.836 −11.042 1.00 57.90 ATOM 4414 C ARG B 979 7.590 16.920 −9.767 1.00 59.18 ATOM 4415 O ARG B 979 7.417 17.834 −8.970 1.00 61.14 ATOM 4416 CB ARG B 979 5.329 16.367 −10.704 1.00 59.68 ATOM 4417 CG ARG B 979 4.322 16.484 −11.856 1.00 61.54 ATOM 4418 CD ARG B 979 3.022 15.725 −11.544 1.00 61.64 ATOM 4419 NE ARG B 979 2.376 15.243 −12.766 1.00 63.13 ATOM 4420 CZ ARG B 979 1.427 14.309 −12.809 1.00 62.83 ATOM 4421 NH1 ARG B 979 0.989 13.740 −11.690 1.00 63.57 ATOM 4422 NH2 ARG B 979 0.931 13.924 −13.980 1.00 62.38 ATOM 4423 N ASP B 980 8.496 15.964 −9.583 1.00 59.01 ATOM 4424 CA ASP B 980 9.384 15.936 −8.422 1.00 59.63 ATOM 4425 C ASP B 980 10.685 15.245 −8.872 1.00 60.07 ATOM 4426 O ASP B 980 11.062 14.183 −8.362 1.00 58.65 ATOM 4427 CB ASP B 980 8.709 15.177 −7.262 1.00 60.54 ATOM 4428 CG ASP B 980 9.456 15.334 −5.922 1.00 62.11 ATOM 4429 OD1 ASP B 980 10.255 16.288 −5.765 1.00 61.29 ATOM 4430 OD2 ASP B 980 9.226 14.502 −5.015 1.00 61.48 ATOM 4431 N PRO B 981 11.392 15.865 −9.837 1.00 59.64 ATOM 4432 CA PRO B 981 12.651 15.412 −10.445 1.00 60.15 ATOM 4433 C PRO B 981 13.831 14.975 −9.573 1.00 60.53 ATOM 4434 O PRO B 981 14.609 14.114 −9.986 1.00 60.77 ATOM 4435 CB PRO B 981 13.025 16.574 −11.372 1.00 58.58 ATOM 4436 CG PRO B 981 12.393 17.753 −10.726 1.00 57.47 ATOM 4437 CD PRO B 981 11.049 17.213 −10.331 1.00 58.74 ATOM 4438 N GLN B 982 13.981 15.558 −8.386 1.00 61.15 ATOM 4439 CA GLN B 982 15.102 15.197 −7.521 1.00 60.07 ATOM 4440 C GLN B 982 14.854 13.919 −6.745 1.00 57.60 ATOM 4441 O GLN B 982 15.774 13.355 −6.167 1.00 56.36 ATOM 4442 CB GLN B 982 15.427 16.339 −6.559 1.00 63.51 ATOM 4443 CG GLN B 982 16.078 17.547 −7.228 1.00 66.46 ATOM 4444 CD GLN B 982 16.277 18.713 −6.272 1.00 69.16 ATOM 4445 OE1 GLN B 982 15.811 18.681 −5.134 1.00 72.71 ATOM 4446 NE2 GLN B 982 16.977 19.745 −6.729 1.00 70.65 ATOM 4447 N ARG B 983 13.607 13.464 −6.745 1.00 56.49 ATOM 4448 CA ARG B 983 13.221 12.230 −6.062 1.00 54.51 ATOM 4449 C ARG B 983 13.456 11.011 −6.955 1.00 52.63 ATOM 4450 O ARG B 983 13.445 9.870 −6.489 1.00 51.88 ATOM 4451 CB ARG B 983 11.741 12.280 −5.693 1.00 54.81 ATOM 4452 CG ARG B 983 11.219 11.016 −5.031 1.00 56.29 ATOM 4453 CD ARG B 983 9.712 11.054 −4.892 1.00 57.50 ATOM 4454 NE ARG B 983 9.214 9.997 −4.018 1.00 58.23 ATOM 4455 CZ ARG B 983 7.924 9.735 −3.834 1.00 57.38 ATOM 4456 NH1 ARG B 983 7.003 10.452 −4.469 1.00 56.60 ATOM 4457 NH2 ARG B 983 7.556 8.765 −3.011 1.00 57.50 ATOM 4458 N TYR B 984 13.673 11.257 −8.241 1.00 50.73 ATOM 4459 CA TYR B 984 13.874 10.166 −9.172 1.00 50.45 ATOM 4460 C TYR B 984 15.240 10.063 −9.855 1.00 48.61 ATOM 4461 O TYR B 984 15.605 8.994 −10.339 1.00 48.45 ATOM 4462 CB TYR B 984 12.724 10.175 −10.177 1.00 49.68 ATOM 4463 CG TYR B 984 11.415 9.906 −9.468 1.00 53.31 ATOM 4464 CD1 TYR B 984 10.591 10.950 −9.047 1.00 54.83 ATOM 4465 CD2 TYR B 984 11.049 8.606 −9.118 1.00 54.60 ATOM 4466 CE1 TYR B 984 9.435 10.703 −8.289 1.00 54.57 ATOM 4467 CE2 TYR B 984 9.902 8.353 −8.361 1.00 55.09 ATOM 4468 CZ TYR B 984 9.106 9.405 −7.952 1.00 54.72 ATOM 4469 OH TYR B 984 7.984 9.146 −7.207 1.00 56.77 ATOM 4470 N LEU B 985 15.996 11.157 −9.878 1.00 46.87 ATOM 4471 CA LEU B 985 17.341 11.160 −10.459 1.00 46.02 ATOM 4472 C LEU B 985 18.272 11.936 −9.519 1.00 46.87 ATOM 4473 O LEU B 985 17.927 13.029 −9.063 1.00 45.27 ATOM 4474 CB LEU B 985 17.344 11.812 −11.845 1.00 44.28 ATOM 4475 CG LEU B 985 16.651 11.099 −13.001 1.00 43.30 ATOM 4476 CD1 LEU B 985 17.075 11.770 −14.289 1.00 43.28 ATOM 4477 CD2 LEU B 985 17.024 9.617 −13.037 1.00 43.77 ATOM 4478 N VAL B 986 19.443 11.372 −9.226 1.00 46.59 ATOM 4479 CA VAL B 986 20.381 12.023 −8.317 1.00 47.28 ATOM 4480 C VAL B 986 21.628 12.479 −9.045 1.00 48.95 ATOM 4481 O VAL B 986 22.479 11.675 −9.419 1.00 50.35 ATOM 4482 CB VAL B 986 20.809 11.087 −7.179 1.00 49.66 ATOM 4483 CG1 VAL B 986 21.654 11.863 −6.171 1.00 48.82 ATOM 4484 CG2 VAL B 986 19.586 10.484 −6.507 1.00 48.62 ATOM 4485 N ILE B 987 21.742 13.786 −9.214 1.00 49.22 ATOM 4486 CA ILE B 987 22.854 14.377 −9.927 1.00 50.44 ATOM 4487 C ILE B 987 23.496 15.472 −9.084 1.00 53.00 ATOM 4488 O ILE B 987 22.797 16.347 −8.568 1.00 53.10 ATOM 4489 CB ILE B 987 22.341 14.991 −11.246 1.00 49.77 ATOM 4490 CG1 ILE B 987 21.671 13.902 −12.087 1.00 50.87 ATOM 4491 CG2 ILE B 987 23.465 15.666 −11.995 1.00 48.64 ATOM 4492 CD1 ILE B 987 20.856 14.444 −13.253 1.00 51.02 ATOM 4493 N GLN B 988 24.820 15.427 −8.946 1.00 55.17 ATOM 4494 CA GLN B 988 25.537 16.446 −8.185 1.00 56.54 ATOM 4495 C GLN B 988 25.166 17.807 −8.757 1.00 58.14 ATOM 4496 O GLN B 988 25.094 17.971 −9.975 1.00 57.08 ATOM 4497 CB GLN B 988 27.047 16.245 −8.300 1.00 57.24 ATOM 4498 CG GLN B 988 27.612 15.195 −7.370 1.00 58.82 ATOM 4499 CD GLN B 988 29.129 15.143 −7.409 1.00 60.42 ATOM 4500 OE1 GLN B 988 29.725 14.831 −8.441 1.00 63.50 ATOM 4501 NE2 GLN B 988 29.763 15.448 −6.282 1.00 62.41 ATOM 4502 N GLY B 989 24.951 18.784 −7.879 1.00 59.86 ATOM 4503 CA GLY B 989 24.562 20.106 −8.332 1.00 62.53 ATOM 4504 C GLY B 989 23.067 20.003 −8.486 1.00 64.69 ATOM 4505 O GLY B 989 22.426 19.366 −7.661 1.00 65.23 ATOM 4506 N ASP B 990 22.494 20.611 −9.516 1.00 67.44 ATOM 4507 CA ASP B 990 21.053 20.475 −9.704 1.00 70.60 ATOM 4508 C ASP B 990 20.352 20.808 −8.377 1.00 72.92 ATOM 4509 O ASP B 990 19.373 20.165 −7.996 1.00 73.02 ATOM 4510 CB ASP B 990 20.764 19.019 −10.136 1.00 68.29 ATOM 4511 CG ASP B 990 19.376 18.821 −10.727 1.00 65.16 ATOM 4512 OD1 ASP B 990 18.904 19.688 −11.493 1.00 64.82 ATOM 4513 OD2 ASP B 990 18.764 17.771 −10.433 1.00 61.33 ATOM 4514 N ALA B 991 20.862 21.814 −7.675 1.00 75.66 ATOM 4515 CA ALA B 991 20.275 22.219 −6.399 1.00 79.01 ATOM 4516 C ALA B 991 19.048 23.107 −6.615 1.00 80.54 ATOM 4517 O ALA B 991 17.965 22.739 −6.100 1.00 81.75 ATOM 4518 CB ALA B 991 21.317 22.948 −5.537 1.00 77.93 ATOM 4519 OXT ALA B 991 19.180 24.153 −7.295 1.00 81.39 ATOM 4520 F1 LIG C 1 −21.453 16.649 −0.604 1.00 65.92 ATOM 4521 C2 LIG C 1 −21.069 17.936 −0.472 1.00 62.88 ATOM 4522 C3 LIG C 1 −19.922 18.287 0.383 1.00 60.99 ATOM 4523 C4 LIG C 1 −19.435 19.703 0.395 1.00 60.35 ATOM 4524 C5 LIG C 1 −20.135 20.740 −0.395 1.00 61.20 ATOM 4525 C6 LIG C 1 −21.331 20.391 −1.193 1.00 63.29 ATOM 4526 C7 LIG C 1 −21.800 18.979 −1.237 1.00 63.70 ATOM 4527 C8 LIG C 1 −18.188 20.151 1.138 1.00 58.87 ATOM 4528 O9 LIG C 1 −17.171 19.172 1.348 1.00 56.77 ATOM 4529 C10 LIG C 1 −16.358 18.640 0.332 1.00 55.56 ATOM 4530 C11 LIG C 1 −15.952 17.241 0.543 1.00 56.41 ATOM 4531 C12 LIG C 1 −15.101 16.562 −0.402 1.00 54.33 ATOM 4532 C13 LIG C 1 −14.603 17.275 −1.616 1.00 53.77 ATOM 4533 C14 LIG C 1 −15.012 18.688 −1.848 1.00 55.54 ATOM 4534 C15 LIG C 1 −15.913 19.352 −0.900 1.00 54.37 ATOM 4535 N16 LIG C 1 −13.762 16.701 −2.549 1.00 49.69 ATOM 4536 C17 LIG C 1 −13.714 15.438 −3.082 1.00 50.51 ATOM 4537 N18 LIG C 1 −14.809 14.489 −2.937 1.00 49.27 ATOM 4538 C19 LIG C 1 −14.740 13.219 −3.533 1.00 49.13 ATOM 4539 N20 LIG C 1 −13.631 12.866 −4.316 1.00 48.53 ATOM 4540 C21 LIG C 1 −12.558 13.784 −4.480 1.00 50.01 ATOM 4541 C22 LIG C 1 −12.550 15.113 −3.834 1.00 50.59 ATOM 4542 S23 LIG C 1 −11.201 16.018 −4.243 1.00 54.32 ATOM 4543 C24 LIG C 1 −10.572 14.794 −5.310 1.00 54.73 ATOM 4544 C25 LIG C 1 −11.377 13.652 −5.309 1.00 52.56 ATOM 4545 CL2 LIG C 1 −16.406 16.290 1.907 1.00 58.80 ATOM 4546 C27 LIG C 1 −8.858 16.177 −6.594 1.00 59.22 ATOM 4547 C26 LIG C 1 −9.449 14.847 −6.122 1.00 55.07 ATOM 4548 F1 LIG D 1 10.853 15.135 −41.543 1.00 58.61 ATOM 4549 C2 LIG D 1 11.037 13.839 −41.713 1.00 54.55 ATOM 4550 C3 LIG D 1 12.223 13.471 −42.454 1.00 54.59 ATOM 4551 C4 LIG D 1 12.685 12.058 −42.421 1.00 55.40 ATOM 4552 C5 LIG D 1 11.870 11.031 −41.722 1.00 55.68 ATOM 4553 C6 LIG D 1 10.584 11.399 −41.086 1.00 55.06 ATOM 4554 C7 LIG D 1 10.166 12.828 −41.075 1.00 55.50 ATOM 4555 C8 LIG D 1 14.013 11.667 −43.046 1.00 55.59 ATOM 4556 O9 LIG D 1 14.925 12.754 −43.284 1.00 54.46 ATOM 4557 C10 LIG D 1 15.752 13.298 −42.283 1.00 54.12 ATOM 4558 C11 LIG D 1 16.205 14.668 −42.540 1.00 54.63 ATOM 4559 C12 LIG D 1 17.138 15.313 −41.638 1.00 54.53 ATOM 4560 C13 LIG D 1 17.592 14.617 −40.390 1.00 54.63 ATOM 4561 C14 LIG D 1 17.151 13.224 −40.122 1.00 54.98 ATOM 4562 C15 LIG D 1 16.212 12.590 −41.043 1.00 53.54 ATOM 4563 N16 LIG D 1 18.380 15.217 −39.444 1.00 52.13 ATOM 4564 C17 LIG D 1 18.311 16.478 −38.879 1.00 52.92 ATOM 4565 N18 LIG D 1 17.153 17.343 −38.997 1.00 52.67 ATOM 4566 C19 LIG D 1 17.111 18.603 −38.359 1.00 52.27 ATOM 4567 N20 LIG D 1 18.197 19.019 −37.573 1.00 52.85 ATOM 4568 C21 LIG D 1 19.370 18.189 −37.471 1.00 53.46 ATOM 4569 C22 LIG D 1 19.449 16.879 −38.137 1.00 52.71 ATOM 4570 S23 LIG D 1 20.838 16.039 −37.751 1.00 55.09 ATOM 4571 C24 LIG D 1 21.417 17.235 −36.656 1.00 55.61 ATOM 4572 C25 LIG D 1 20.602 18.381 −36.703 1.00 54.95 ATOM 4573 CL2 LIG D 1 15.733 15.611 −43.921 1.00 56.18 ATOM 4574 C27 LIG D 1 23.036 15.744 −35.342 1.00 59.16 ATOM 4575 C26 LIG D 1 22.474 17.108 −35.765 1.00 54.82 ATOM 4576 O HOH E 1 −7.599 8.623 −13.123 1.00 62.46 ATOM 4577 O HOH E 2 24.517 23.513 −28.035 1.00 64.27 ATOM 4578 O HOH E 3 −20.296 13.666 15.285 1.00 63.01 ATOM 4579 O HOH E 4 −22.374 8.176 −7.192 1.00 49.42 ATOM 4580 O HOH E 5 −29.264 30.402 −15.340 1.00 37.27 ATOM 4581 O HOH E 6 −15.548 26.298 −3.002 1.00 60.28 ATOM 4582 O HOH E 7 −16.488 46.164 −1.672 1.00 37.96 ATOM 4583 O HOH E 8 −23.337 42.864 −22.019 1.00 54.63 ATOM 4584 O HOH E 9 11.610 18.211 −56.805 1.00 64.90 ATOM 4585 O HOH E 10 16.106 5.158 −39.459 1.00 71.20 ATOM 4586 O HOH E 11 24.422 −1.900 −32.376 1.00 37.06 ATOM 4587 O HOH E 12 18.940 −3.777 −26.629 1.00 37.73 ATOM 4588 O HOH E 13 2.846 1.640 −26.716 1.00 48.90 ATOM 4589 O HOH E 14 22.115 6.710 −30.625 1.00 46.15 ATOM 4590 O HOH E 15 27.166 −0.416 −20.681 1.00 52.66 ATOM 4591 O HOH E 16 27.370 0.625 −28.338 1.00 48.54 ATOM 4592 O HOH E 17 8.879 −10.943 −20.472 1.00 43.79 ATOM 4593 O HOH E 18 22.979 20.646 −12.884 1.00 55.83 ATOM 4594 O HOH E 19 −23.835 38.304 −2.575 1.00 46.63 ATOM 4595 O HOH E 20 3.858 19.802 −44.299 1.00 51.25 ATOM 4596 O HOH E 21 6.565 20.312 −34.549 1.00 67.07 ATOM 4597 O HOH E 22 6.762 22.561 −32.466 1.00 63.76 ATOM 4598 O HOH E 23 17.087 2.388 −32.802 1.00 50.29 ATOM 4599 O HOH E 24 19.085 −5.539 −28.680 1.00 47.97 ATOM 4600 O HOH E 25 8.303 −6.214 −39.578 1.00 53.88 ATOM 4601 O HOH E 26 24.363 7.903 −14.629 1.00 43.74 ATOM 4602 O HOH E 27 −27.032 11.186 2.400 1.00 74.22 ATOM 4603 O HOH E 28 −12.942 20.542 −5.335 1.00 44.65 ATOM 4604 O HOH E 29 −7.825 34.064 −9.696 1.00 36.01 ATOM 4605 O HOH E 30 6.161 13.446 −8.135 1.00 48.06 ATOM 4606 O HOH E 31 4.895 21.272 −54.439 1.00 37.34 ATOM 4607 O HOH E 32 14.560 16.150 −38.934 1.00 49.73 ATOM 4608 O HOH E 33 −17.191 16.196 −2.787 1.00 49.94 ATOM 4609 O HOH E 34 −12.431 16.753 −33.087 1.00 50.01 ATOM 4610 O HOH E 35 19.316 15.273 −8.990 1.00 41.76 ATOM 4611 O HOH E 36 22.919 −2.802 −12.770 1.00 32.09 ATOM 4612 O HOH E 37 −20.465 42.538 −22.926 1.00 48.88 ATOM 4613 O HOH E 38 24.551 −2.864 −35.433 1.00 38.92 ATOM 4614 O HOH E 39 10.469 2.554 −40.581 1.00 54.18 ATOM 4615 O HOH E 40 4.881 19.023 −24.625 1.00 58.60 ATOM 4616 O HOH E 41 18.317 10.202 −53.601 1.00 71.11 ATOM 4617 O HOH E 42 −13.865 22.064 10.271 1.00 57.28 ATOM 4618 O HOH E 43 −35.587 21.497 3.030 1.00 36.88 ATOM 4619 O HOH E 44 −26.803 14.899 −5.791 1.00 40.87 ATOM 4620 O HOH E 45 −24.968 8.964 −9.528 1.00 60.43 ATOM 4621 O HOH E 46 −18.782 34.826 −10.499 1.00 37.91 ATOM 4622 O HOH E 47 −15.030 29.928 −8.619 1.00 52.85 ATOM 4623 O HOH E 48 −19.234 30.472 −9.478 1.00 49.50 ATOM 4624 O HOH E 49 −10.976 11.240 12.729 1.00 52.40 ATOM 4625 O HOH E 50 16.214 −4.944 −38.622 1.00 53.39 ATOM 4626 O HOH E 51 −14.354 32.711 −8.242 1.00 47.04 ATOM 4627 O HOH E 52 −13.127 35.963 −19.946 1.00 44.74 ATOM 4628 O HOH E 53 −26.260 30.450 −26.299 1.00 46.29 ATOM 4629 O HOH E 54 9.344 23.549 −34.825 1.00 60.48 ATOM 4630 O HOH E 55 12.830 1.506 −32.483 1.00 44.17 END

REFERENCES

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1. An ErbB4 kinase domain in liganded crystalline form, comprising the amino acid sequence of SEQ ID NO: 1 and having the structural coordinates of Table
 2. 2. A liganded ErbB4 kinase domain as claimed in claim 1, wherein the crystalline form has lattice constants of a=63.95 Å, b=63.95 Å, c=163.95 Å, α=90°, β=90°, and γ=90°.
 3. A liganded ErbB4 kinase domain in crystalline form as claimed in claim 1, wherein said crystalline form has a space group of P4₃.
 4. A method of ErbB4 inhibitor design, comprising: generating a three dimensional computer model which represents ErbB4 kinase domain in liganded form, said kinase domain described by the amino acid sequence of SEQ ID NO: 1 and having the structural coordinates of Table 2; evaluating compounds as potential ErbB4 inhibitors using said model; and selecting compounds for further testing based on said evaluation.
 5. A method of ErbB4 inhibitor design, comprising: generating a three dimensional computer model which represents a ErbB4 kinase domain in liganded form, said kinase domain described by the amino acid sequence of SEQ ID NO: 1 and having the structural coordinates of Table 2; evaluating compounds as potential ErbB4 inhibitors using said model; wherein said evaluation comprises identifying compounds capable of at least one of the following ErbB4 kinase domain/compound interactions: (iv) one or more interactions with amino acid residues of the ErbB4 kinase domain hinge region; (v) one or more interactions with amino acid residues of the ErbB4 kinase domain adenine pocket, (iii) one or more interactions with amino acid residues of the ErbB4 kinase sugar pocket, (iv) one or more interactions with amino acid residues of the ErbB4 kinase domain back pocket, and (v) one or more interactions with amino acid residues of the ErbB4 kinase domain solvent interface; and selecting compounds for further testing based on said evaluation.
 6. A method of ErbB4 inhibitor design, comprising: generating a three dimensional computer model which represents a ErbB4 kinase domain in liganded form, said kinase domain described by the amino acid sequence of SEQ ID NO: 1 and having the structural coordinates of Table 2; evaluating compounds as potential ErbB4 inhibitors using said model; wherein said evaluation comprises identifying compounds capable of at least one of the following ErbB4 kinase domain/compound interactions: (i) one or more interactions with amino acid residues 796, 797, 798, 799, and 800; (ii) one or more interactions with amino acid residues 724, 749, and 850; (iii) one or more interactions with amino acid residues 848, 860, 803, 847, 732, and 725; (iv) one or more interactions with amino acid residues 732, 749, 751, 796, 861, 860, 772, 781, 783, 794, 796, and 862; and (v) one or more interactions with residues 801, 802, 803, 806, and 810; and selecting compounds for further testing based on said evaluation.
 7. A method of treating a disorder characterized by inappropriate ErbB4 activity in a mammal, comprising: administering to said mammal a therapeutically effective amount of a compound that can form a complex with a ErbB4 kinase domain thereby resulting in a ErbB4 kinase domain in liganded form, said kinase domain in liganded form being described by the amino acid sequence of SEQ ID NO: 1 and the structural coordinates of Table 2, wherein said complex is characterized by at least one of the following ErbB4 kinase domain/compound interactions: (i) one or more interactions with amino acid residues of the ErbB4 kinase domain hinge region; (ii) one or more interactions with amino acid residues of the ErbB4 kinase domain adenine pocket, (iii) one or more interactions with amino acid residues of the ErbB4 kinase sugar pocket and phosphate region, (iv) one or more interactions with amino acid residues of the ErbB4 kinase domain back pocket, and (v) one or more interactions with amino acid residues of the ErbB4 kinase domain solvent interface.
 8. A method of inhibiting ErbB4 in a mammal, comprising: administering to said mammal a therapeutically effective amount of a compound that can form a complex with a ErbB4 kinase domain thereby resulting in a ErbB4 kinase domain in liganded form, said kinase domain in liganded form being described by the amino acid sequence of SEQ ID NO: 1 and the structural coordinates of Table 2, wherein said complex is characterized by at least one of the following ErbB4 kinase domain/compound interactions: (i) one or more interactions with amino acid residues of the ErbB4 kinase domain hinge region; (ii) one or more interactions with amino acid residues of the ErbB4 kinase domain adenine pocket, (iii) one or more interactions with amino acid residues of the ErbB4 kinase sugar pocket and phosphate region, (iv) one or more interactions with amino acid residues of the ErbB4 kinase domain back pocket, and (v) one or more interactions with amino acid residues of the ErbB4 kinase domain solvent interface.
 9. An ErbB4 kinase domain/inhibitor complex, comprising: an ErbB4 kinase domain form being described by the amino acid sequence of SEQ ID NO: 1 and the structural coordinates of Table 2 and a compound that can form a complex with the ErbB4 kinase domain said complex is characterized by at least one of the following ErbB4 kinase domain/compound interactions: (i) one or more interactions with amino acid residues of the ErbB4 kinase domain hinge region; (ii) one or more interactions with amino acid residues of the ErbB4 kinase domain adenine pocket, (iii) one or more interactions with amino acid residues of the ErbB4 kinase sugar pocket and phosphate region, (iv) one or more interactions with amino acid residues of the ErbB4 kinase domain back pocket, and (v) one or more interactions with amino acid residues of the ErbB4 kinase domain solvent interface. 